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Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by GCS.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1501 | 0 | 0 | 1311 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1395-1395 HART PS; OLSON SM; CRANDALL K; TARLETON J FRAGILE-X SYNDROME RESULTING FROM A 400 BASEPAIR DELETION WITHIN THE FMR1 GENE | 0 | 2 |
| 1502 | 0 | 30 | 1345 1995 BIOSPECTROSCOPY 1(4):235-245 CARMONA P; MOLINA M; LASAGABASTER A; ESCOBAR R DETERMINATION OF THE HYDROGEN-BONDED STRUCTURE OF CGG TRIMERS IN CHLOROFORM SOLUTION BY VIBRATIONAL SPECTROSCOPY | 0 | 2 |
| 1503 | 45 | 78 | 1355 1995 CLINICS IN LABORATORY MEDICINE 15(4):859-& Brown WT Perspectives and molecular diagnosis of the fragile X syndrome | 2 | 2 |
| 1504 | 18 | 26 | 1369 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):302-309 Holden JJA; Chalifoux M; Wing M; JulienInalsingh C; Scott E; et al. Distribution and frequency of FMR1 CGG repeat number in institutionalized developmentally disabled individuals | 0 | 2 |
| 1505 | 5 | 9 | 1380 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):408-410 HowardPeebles PN; Maddalena A; Black SH; Levinson G; Bick DP; et al. Fragile X screening in pediatric and obstetrical patients | 2 | 2 |
| 1506 | 12 | 26 | 1392 1995 GENETIC EPIDEMIOLOGY 12(3):279-290 HUGGINS RM; LOESCH DZ USE OF ROBUST STATISTICAL-METHODS TO DETERMINE THE EFFECT OF FRAGILE-X ON MEANS AND VARIANCE-COMPONENTS OF A QUANTITATIVE TRAIT | 1 | 2 |
| 1507 | 0 | 0 | 1411 1995 JOURNAL OF MEDICAL GENETICS 32(2):144-145 MORTON JE; RINDL PM; BULLOCK S; BUNDEY S; WEBB T FRAGILE-X SYNDROME IS LESS COMMON THAN PREVIOUSLY ESTIMATED | 2 | 2 |
| 1508 | 9 | 10 | 1459 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):187-190 Grasso M; Perroni L; Colella S; Piombo G; Argusti A; et al. Prenatal diagnosis of 30 fetuses at risk for fragile X syndrome | 1 | 2 |
| 1509 | 28 | 77 | 1575 1996 SCREENING 4(4):175-192 Meadows KL; Sherman SL Fragile X syndrome: Examination of issues pertaining to population-based screening | 2 | 2 |
| 1510 | 0 | 0 | 1612 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A316-A316 Nolin SL; Houck GE; Blumstein H; Ye LL; Dobkin CS; et al. Single cell analysis shows different FMR1 CGG repeat stability in sperm and lymphocytes of premutation males. | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1511 | 27 | 35 | 1640 1997 BRAZILIAN JOURNAL OF GENETICS 20(4):731-739 Mingroni-Netto RC; Pavanello RCM; Otto PA; Vianna-Morgante AM Experience with molecular and cytogenetic diagnosis of fragile X syndrome in Brazilian families | 2 | 2 |
| 1512 | 10 | 16 | 1651 1997 DIAGNOSTIC MOLECULAR PATHOLOGY 6(3):161-166 Marini T; Pflueger S; Jackson A; Naber S; Karpells S; et al. A five-year experience with fragile X testing - Setting laboratory standards of practice and a cost-effective protocol | 1 | 2 |
| 1513 | 1 | 1 | 1697 1997 NATURE STRUCTURAL BIOLOGY 4(10):840-840 Musco G; Kharrat A; Stier G; Fraternali F; Gibson TJ; et al. The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome (vol 4, pg 712, 1997) | 1 | 2 |
| 1514 | 20 | 30 | 1720 1998 ANNALS OF HUMAN GENETICS 62:337-347 Huggins RM; Loesch DZ; Sherman SL A branching non-linear autoregressive model for the transmission of the fragile X dynamic repeat mutation | 1 | 2 |
| 1515 | 15 | 21 | 1725 1998 CLINICAL CHEMISTRY AND LABORATORY MEDICINE 36(8):649-653 Poon PMK; Chen QL; Lai KYC; Wong CK; Pang CP CGG repeat interruptions in the FMR1 gene in patients with infantile autism | 0 | 2 |
| 1516 | 23 | 30 | 1741 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6(5):518-522 Peixoto A; dos Santos MR; Seruca R; Amorim A; Castedo S Analysis of FMR1 and flanking microsatellite markers in normal and fragile X chromosomes in Portugal: evidence for a "protector" haplotype | 2 | 2 |
| 1517 | 2 | 88 | 1786 1998 MEDICAL HYPOTHESES 51(3):223-233 Fischer KM Expanded (CAG)(n), (CGG)(n) and (GAA)(n) trinucleotide repeat microsatellites, and mutant purine synthesis and pigmentation genes cause schizophrenia and autism | 0 | 2 |
| 1518 | 4 | 9 | 1829 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):281-285 Teisl JT; Reiss AL; Mazzocco MMM Maximizing the sensitivity of a screening questionnaire for determining fragile X at-risk status | 2 | 2 |
| 1519 | 4 | 28 | 1832 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):298-301 Kotilainen J; Pirinen S Dental maturity is advanced in fragile X syndrome | 2 | 2 |
| 1520 | 8 | 14 | 1842 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):342-346 Jenkins EC; Wen GY; Kim KS; Zhong N; Sapienza VJ; et al. Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1521 | 13 | 22 | 1852 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):217-220 Patsalis PC; Sismani C; Stylianou S; Ioannou P; Joseph G; et al. Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population | 1 | 2 |
| 1522 | 35 | 50 | 1882 1999 CURRENT OPINION IN PSYCHIATRY 12(5):573-578 Harris SW; Hagerman RJ Fragile X syndrome: new developments | 2 | 2 |
| 1523 | 13 | 21 | 1894 1999 GENETIC TESTING 3(3):301-304 Melis MA; Addis M; Lepiani C; Congeddu E; Cossu P; et al. A strategy for fragile-X carrier screening | 0 | 2 |
| 1524 | 3 | 8 | 1895 1999 GENETICS AND MOLECULAR BIOLOGY 22(2):169-172 Pena SDJ; Sturzeneker R Diagnosis of the fragile X syndrome in males using methylation-specific PCR of the FMR1 locus | 0 | 2 |
| 1525 | 2 | 5 | 1916 1999 JOURNAL OF MEDICAL GENETICS 36(2):171-171 Macpherson J; Murray A; Webb J; Jacobs P Fragile X syndrome: of POF and premutations | 1 | 2 |
| 1526 | 7 | 113 | 1925 1999 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 5(4):305-313 Hagerman RJ Psychopharmacological interventions in fragile X syndrome, fetal alcohol syndrome, Prader-Willi syndrome, Angelman syndrome, Smith-Magenis syndrome, and velocardiofacial syndrome | 0 | 2 |
| 1527 | 0 | 0 | 1942 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):18-18 Jin P; Feng Y; Brown V; Warren ST Identification of polyribosomes-associated mRNAs regulated by fragile X mental retardation protein (FMRP) using oligonucleotide microarrays. | 1 | 2 |
| 1528 | 4 | 9 | 1977 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(5):516-517 Limprasert P; Jaruratanasirikul S; Vasiknanonte P Unilateral macroorchidism in fragile X syndrome | 2 | 2 |
| 1529 | 9 | 19 | 1988 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 275(2):608-610 Beaulieu MA A distinct FMRP polysomal population at an advanced stage of mammalian erythropoiesis | 2 | 2 |
| 1530 | 1 | 6 | 2003 2000 CYTOGENETICS AND CELL GENETICS 89(1-2):11-13 Bardoni B; Giglio S; Schenck A; Rocchi M; Mandel JL Assignment of NUFIP1 (Nuclear FMRP Interacting Protein 1) gene to chromosome 13q14 and assignment of a pseudogene to chromosome 6q12 | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1531 | 23 | 46 | 2004 2000 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 42(11):768-774 Sheldon L; Turk J Monozygotic boys with fragile X syndrome | 1 | 2 |
| 1532 | 31 | 44 | 2016 2000 GENETICS IN MEDICINE 2(4):242-248 Burman RW; Anoe KS; Popovich BW Fragile X full mutations ave more similar in siblings than in unrelated patients: further evidence for a familial factor in CGG repeat dynamics | 1 | 2 |
| 1533 | 6 | 14 | 2081 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 74(1):80-93 Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; et al. Evidence for altered fragile-x mental retardation protein expression in response to behavioral stimulation (vol 73, pg 87, 2000) | 2 | 2 |
| 1534 | 15 | 32 | 2116 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(3):226-230 Schultz-Pedersen S; Hasle H; Olsen JH; Friedrich U Evidence of decreased risk of cancer in individuals with fragile X | 0 | 2 |
| 1535 | 9 | 25 | 2141 2001 COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING 4(3):265-272 Murray J; Cuckle H Cystic fibrosis and fragile X syndrome: The arguments for antenatal screening | 1 | 2 |
| 1536 | 65 | 108 | 2183 2001 MOLECULAR GENETICS AND METABOLISM 74(1-2):89-97 Hagerman RJ; Hagerman PJ Fragile X syndrome: A model of gene-brain-behavior relationships | 1 | 2 |
| 1537 | 13 | 30 | 2200 2001 REVISTA DE NEUROLOGIA 33:S24-S29 Cornish K; Munir F; Wilding J A neuropsychological and behavioural profile of a attention deficits in fragile X syndrome | 2 | 2 |
| 1538 | 0 | 0 | 2218 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):185-185 Jacquemont S; Hagerman RJ; Leehey M; Greco C; Brunberg J; et al. Characterization of a progressive neurological condition in older adult male carriers of the fragile X premutation. | 2 | 2 |
| 1539 | 3 | 36 | 2241 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 111(4):381-387 Steinhausen HC; von Gontard A; Spohr HL; Hauffa BP; Eiholzer U; et al. Behavioral phenotypes in four mental retardation syndromes: Fetal alcohol syndrome, Prader-Willi syndrome, fragile X syndrome, and tuberosis sclerosis | 0 | 2 |
| 1540 | 14 | 57 | 2263 2002 DEVELOPMENTAL PSYCHOBIOLOGY 41(2):133-146 Keysor CS; Mazzocco MMM; McLeod DR; Hoehn-Saric R Physiological arousal in females with fragile X or Turner syndrome | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1541 | 10 | 13 | 2308 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):131-134 Kaufmann WE Neurobiology of fragile X syndrome: From molecular genetics to neurobehavioral phenotype | 0 | 2 |
| 1542 | 15 | 20 | 2310 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):145-147 Feng Y Fragile X mental retardation: Misregulation of protein synthesis in the developing brain? | 2 | 2 |
| 1543 | 29 | 60 | 2386 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(5):314-326 Demark JL; Feldman MA; Holden JJA Behavioral relationship between autism and fragile X syndrome | 1 | 2 |
| 1544 | 20 | 38 | 2407 2003 BRAIN TOPOGRAPHY 15(3):165-171 Castren M; Paakkonen A; Tarkka IM; Ryynanen M; Partanen J Augmentation of auditory N1 in children with fragile X syndrome | 2 | 2 |
| 1545 | 20 | 29 | 2422 2003 GENETIC TESTING 7(4):339-343 Rife M; Badenas C; Mallolas J; Jimenez L; Cervera R; et al. Incidence of Fragile X in 5,000 consecutive newborn males | 0 | 2 |
| 1546 | 34 | 43 | 2427 2003 HUMAN GENETICS 113(5):371-376 Arocena DG; Breece KE; Hagerman PJ Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population | 1 | 2 |
| 1547 | 7 | 10 | 2462 2003 NEURON 38(6):843-845 Billuart P; Chelly J From fragile X mental retardation protein to Rac1 GTPase: New insights from fly CYFIP | 1 | 2 |
| 1548 | 14 | 26 | 2466 2003 NEUROSCIENCE 119(1):9-13 D'Antuono M; Merlo D; Avoli M Involvement of cholinergic and GABAergic systems in the fragile X knockout mice | 0 | 2 |
| 1549 | 21 | 48 | 2488 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 126A(1):9-17 Kau ASM; Tierney E; Bukelis I; Stump MH; Kates WR; et al. Social behavior profile in young males with fragile X syndrome: Characteristics and specificity | 0 | 2 |
| 1550 | 28 | 62 | 2501 2004 BRAIN 127:591-601 Kogan CS; Boutet I; Cornish K; Zangenehpour S; Mullen KT; et al. Differential impact of the FMR1 gene on visual processing in fragile X syndrome | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1551 | 60 | 135 | 2506 2004 CELLULAR AND MOLECULAR LIFE SCIENCES 61(14):1714-1728 Denman RB; Dolzhanskaya N; Sung YJ Regulating a translational regulator: mechanisms cells use to control the activity of the fragile X mental retardation protein | 1 | 2 |
| 1552 | 20 | 37 | 2510 2004 CURRENT BIOLOGY 14(20):1863-1870 Pan LY; Zhang YQ; Woodruff E; Broadie K The Drosophila fragile X gene negatively regulates neuronal elaboration and synaptic differentiation | 2 | 2 |
| 1553 | 5 | 50 | 2535 2004 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 34(1):41-48 Seltzer MM; Abbeduto L; Krauss MW; Greenberg J; Swe A Comparison groups in autism family research: Down syndrome, fragile X syndrome, and schizophrenia | 0 | 2 |
| 1554 | 12 | 15 | 2554 2004 JOURNAL OF MEDICAL GENETICS 41(4) Tassone F; Hagerman RJ; Garcia-Arocena D; Khandjian EW; Greco CM; et al. Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome | 0 | 2 |
| 1555 | 39 | 74 | 2569 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):17-24 Hessl D; Rivera SM; Reiss AL The neuroanatomy and neuroendocrinotogy of fragile X syndrome | 1 | 2 |
| 1556 | 24 | 54 | 2574 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):53-59 Beckel-Mitchener A; Greenough WT Correlates across the structural, functional, and molecular phenotypes of fragile X syndrome | 0 | 2 |
| 1557 | 17 | 41 | 2602 2004 NUCLEIC ACIDS RESEARCH 32(1):298-306 Fojtik P; Kejnovska I; Vorlickova M The guanine-rich fragile X chromosome repeats are reluctant to form tetraplexes | 0 | 2 |
| 1558 | 0 | 0 | 10 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A100-A100 CARPENTER NJ; LEICHTMAN LG; LOGAN A; SAY B FRAGILE X-LINKED MENTAL-RETARDATION | 1 | 1 |
| 1559 | 0 | 0 | 11 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A107-A107 HOWARDPEEBLES PN; FINLEY WH TESTICULAR AND CYTOGENETIC SCREENING OF RETARDED MALES FROM THE SOUTH FOR THE FRAGILE X-LINKED MENTAL-RETARDATION SYNDROME | 1 | 1 |
| 1560 | 0 | 0 | 12 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A122-A122 SHAPIRO LR; KUHR MD; WILMOT PL; LILIENTHAL ER; HIGGS LC MULTIPLE SIBLING MENTAL-RETARDATION AND THE IMPACT OF THE FRAGILE X-CHROMOSOME | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1561 | 0 | 0 | 18 1981 CLINICAL GENETICS 19(6):493-493 NIELSEN KB; TOMMERUP N; POULSEN H; MIKKELSEN M DANISH FAMILIES WITH X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOME | 1 | 1 |
| 1562 | 0 | 0 | 35 1981 PEDIATRIC RESEARCH 15(4):569-569 SHAPIRO LR; KUHR MD; WILMOT PL MULTIPLE SIBLING MENTAL-RETARDATION AND THE IMPACT OF THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1563 | 0 | 0 | 36 1981 PEDIATRIC RESEARCH 15(4):645-645 PUESCHEL SM; HAYS R; MENDOZA T A FAMILIAL X-LINKED MENTAL-RETARDATION SYNDROME ASSOCIATED WITH MULTIPLE CONGENITAL-ANOMALIES, MEGALOGENITALIA AND A FRAGILE X-CHROMOSOME | 1 | 1 |
| 1564 | 0 | 0 | 42 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A93-A93 HAVKIN S; CHAKI R; GOLDMAN B FRAGILE X-CHROMOSOME IN 2 FAMILIES WITH X-LINKED MENTAL-RETARDATION | 1 | 1 |
| 1565 | 0 | 0 | 43 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A103-A103 NOLIN S; BROWN T; JENKINS E FRAGILE-X SYNDROME - DILEMMAS FOR GENETIC-COUNSELING | 1 | 1 |
| 1566 | 0 | 0 | 45 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A121-A121 CHUDLEY AE; KNOLL J; GERRARD JW; SHEPEL L; MCGAHEY E; et al. FRAGILE X-LINKED MENTAL-RETARDATION - EFFECT OF AGE AND INTELLIGENCE ON EXPRESSION OF FRAGILE-X | 1 | 1 |
| 1567 | 0 | 0 | 48 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A131-A131 KNOLL J; CHUDLEY AE; GERRARD JW EFFICACY OF FUDR IN ENHANCING EXPRESSION OF FRA(X) IN AFFECTED MALES AND CARRIER FEMALES WITH FRAGILE X-LINKED MENTAL-RETARDATION | 1 | 1 |
| 1568 | 0 | 0 | 59 1982 CLINICAL RESEARCH 30(5):A891-A891 MIXON C; DEV V EFFECT OF FUDR AND METHIONINE ON THE EXPRESSION OF FRAGILE X IN A LYMPHOBLASTOID CELL-LINE | 1 | 1 |
| 1569 | 0 | 0 | 60 1982 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 24(2):252-253 SERGOVICH F; POZSONYI J; HINTON GG RECENT ADVANCES IN MENTAL-RETARDATION - THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1570 | 1 | 5 | 61 1982 HOSPITAL PRACTICE 17(7):17-& BROWN WT; JENKINS EC FRAGILE X - ITS DETECTABILITY | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1571 | 0 | 0 | 85 1982 PEDIATRICS 69(5):669-669 GERALD PS X-LINKED MENTAL-RETARDATION AND FRAGILE-X OR MARKER-X SYNDROME - REPLY | 1 | 1 |
| 1572 | 0 | 21 | 88 1982 WIENER KLINISCHE WOCHENSCHRIFT 94(8):217-219 FONATSCH C; FLATZ SD FRAGILE X-CHROMOSOME AND X-LINKED MENTAL-RETARDATION | 1 | 1 |
| 1573 | 0 | 0 | 123 1983 CLINICAL GENETICS 23(3):236-236 PAJARES IL; DELICADO A; GALLEGO A; CASTROVIEJO IP FAMILIAL X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOMES IN 6 SPANISH FAMILIES | 1 | 1 |
| 1574 | 0 | 0 | 124 1983 CLINICAL GENETICS 23(3):241-241 NIELSEN KB; TOMMERUP N; MIKKELSEN M CLINICAL AND CYTOGENETIC FINDINGS IN 26 MENTALLY-RETARDED MALES WITH THE FRAGILE-X | 1 | 1 |
| 1575 | 0 | 0 | 125 1983 CLINICAL GENETICS 23(3):250-251 TEJADA I; NICOLAS H; CHERUY C; BOUE J STUDY OF A LARGE SIBSHIP WITH MENTALLY-RETARDED MALES AND FEMALES CARRYING FRAGILE-X | 1 | 1 |
| 1576 | 1 | 6 | 193 1984 CHINESE MEDICAL JOURNAL 97(11):861-864 XU BZ; REN S; XIAO GF; ZHOU XT A FRAGILE X SYNDROME FAMILY | 0 | 1 |
| 1577 | 1 | 5 | 256 1985 AMERICAN JOURNAL OF PUBLIC HEALTH 75(7):715-716 MILUNSKY A AN IMPORTANT CLINICAL APPROACH IN DETECTING THE FRAGILE X-SYNDROME | 0 | 1 |
| 1578 | 0 | 0 | 264 1985 CLINICAL GENETICS 27(3):307-307 FRYNS JP THE FRAGILE-X SYNDROME - A STUDY OF 83 INDEX-PATIENTS AND THEIR FAMILIES | 0 | 1 |
| 1579 | 3 | 6 | 270 1985 CLINICAL GENETICS 28(5):399-400 SOUDEK D DECREASE OF FRAGILE X-FREQUENCY IN STORED-BLOOD SAMPLES - INDIVIDUAL VARIABILITY | 1 | 1 |
| 1580 | 3 | 5 | 291 1985 HUMAN GENETICS 71(2):182-182 PEMBREY ME; WINTER RM FURTHER SEGREGATION ANALYSIS OF THE FRAGILE X-SYNDROME WITH SPECIAL REFERENCE TO TRANSMITTING MALES | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1581 | 2 | 3 | 292 1985 HUMAN GENETICS 71(2):183-183 SHERMAN SL; JACOBS PA; MORTON NE FURTHER SEGREGATION ANALYSIS OF THE FRAGILE X-SYNDROME WITH SPECIAL REFERENCE TO TRANSMITTING MALES - REPLY | 1 | 1 |
| 1582 | 2 | 2 | 297 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(5):322-322 KERBESHIAN J; BURD L; MARTSOLF JT THE MULTIPOTENTIAL OUTCOME OF FRAGILE X-SYNDROME | 1 | 1 |
| 1583 | 1 | 6 | 304 1985 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 24(2):239-240 HAGERMAN RJ; JACKSON AW AUTISM OR FRAGILE-X SYNDROME | 0 | 1 |
| 1584 | 1 | 7 | 317 1986 AMERICAN JOURNAL OF DISEASES OF CHILDREN 140(4):327-328 HAGERMAN RJ FRAGILE-X SYNDROME AND LEARNING-DISABILITIES - REPLY | 1 | 1 |
| 1585 | 0 | 0 | 358 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 25(1):186-187 DAR H; BAREL H; JAFFE M; WINTER ST THE FRAGILE-X SYNDROME - THE DILEMMA OF SELECTING PATIENTS FOR EXAMINATION | 0 | 1 |
| 1586 | 16 | 37 | 374 1986 CHILD STUDY JOURNAL 16(4):285-296 BURD L; KERBESHIAN J FRAGILE X-SYNDROME - DEVELOPMENTAL ASPECTS | 0 | 1 |
| 1587 | 0 | 0 | 379 1986 CLINICAL GENETICS 29(5):462-462 GOONEWARDENA P; GUSTAVSON KH; HOLMGREN G; TOLUN A; CHOTAI J; et al. STUDIES ON FRAGILE X-MENTAL RETARDATION BY THE USE OF DNA PROBES | 1 | 1 |
| 1588 | 1 | 1 | 417 1987 AMERICAN JOURNAL OF DISEASES OF CHILDREN 141(6):601-602 HAGERMAN RJ POSSIBLE SIMILARITIES BETWEEN THE FRAGILE-X AND ASPERGERS SYNDROMES - REPLY | 1 | 1 |
| 1589 | 10 | 29 | 437 1987 CLINICAL CHEMISTRY 33(10):1726-1730 THIBODEAU SN USE OF RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM ANALYSIS FOR DETECTING CARRIERS OF FRAGILE-X SYNDROME | 1 | 1 |
| 1590 | 12 | 23 | 443 1987 CYTOGENETICS AND CELL GENETICS 44(2-3):118-122 LIN MS; SHIMANUKI K; WILSON MG EXPRESSION OF FRAGILE-X IN HUMAN-MOUSE SOMATIC-CELL HYBRIDS | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1591 | 0 | 0 | 478 1987 JOURNAL OF MEDICAL GENETICS 24(10):640-640 SENIOR J; KILPATRICK M; WEBB T COMPARATIVE LINKAGE STUDIES IN THE FRAGILE X-SYNDROME | 1 | 1 |
| 1592 | 0 | 0 | 479 1987 JOURNAL OF MEDICAL GENETICS 24(10):641-641 HULTEN M; JOHANNISSON R MEIOSIS IN THE FRAGILE-X MENTAL-RETARDATION SYNDROME | 1 | 1 |
| 1593 | 2 | 4 | 481 1987 JOURNAL OF MENTAL DEFICIENCY RESEARCH 31:81-85 COWIE VA; SINGH KR; WHEATER R; BIRD J THE FRAGILE-X SYNDROME IN TWIN SISTERS | 1 | 1 |
| 1594 | 0 | 1 | 489 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 TURNER G THE FRAGILE X-CHROMOSOME - REPLY | 1 | 1 |
| 1595 | 0 | 0 | 490 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 HECHT F; HECHT BK THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1596 | 4 | 4 | 491 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 BURD L THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1597 | 0 | 0 | 494 1987 PRACTITIONER 231(1431):910-& BUNDEY S THE FRAGILE X-SYNDROME | 1 | 1 |
| 1598 | 0 | 0 | 505 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):20-21 KEREM B; GOITEIN R; SCHAAP T THE DISTRIBUTION OF FRAGILE-X CHROMOSOMES IN AMNIOTIC CELLS CULTURED BY THE INSITU TECHNIQUE | 1 | 1 |
| 1599 | 0 | 0 | 510 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):25-25 TOMMERUP N; REINTOFT I; RESKENIELSEN E; BRONDUMNIELSEN K; MIKKELSEN M UNSUSPECTED PRENATAL-DIAGNOSIS OF THE FRAGILE-X | 0 | 1 |
| 1600 | 196 | 429 | 513 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):31-60 SPANO LM; OPITZ JM BIBLIOGRAPHY ON X-LINKED MENTAL-RETARDATION, THE FRAGILE-X AND RELATED SUBJECTS-IV (1988) | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1601 | 1 | 3 | 524 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):201-205 BROWN WT; RUDELLI RD; WISNIEWSKI HM FRAGILE-X SYNDROME - NEUROPATHOLOGY CENTER | 1 | 1 |
| 1602 | 1 | 3 | 540 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):455-457 HOWARDPEEBLES P; FROSTERISKENIUS U FRAGILE-X TESTING IN MOTHERS OF TRANSMITTING MALES | 0 | 1 |
| 1603 | 6 | 13 | 574 1988 CLINICAL GENETICS 33(3):169-175 LOESCH DZ DISCRIMINANT-ANALYSIS OF DERMATOGLYPHIC MEASUREMENTS IN FRAGILE-X MALES AND FEMALES | 0 | 1 |
| 1604 | 10 | 48 | 592 1988 HUMAN GENETICS 79(4):341-346 VANDAMME B; LIEBAERS I; HENS L; BERNHEIM JL; ROOBOL C THE ROLE OF FLUORINATED PYRIMIDINE ANALOGS IN THE INDUCTION OF THE INVITRO EXPRESSION OF THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1605 | 27 | 63 | 612 1988 QUARTERLY JOURNAL OF MEDICINE 69(258):755-763 FROSTERISKENIUS U; PATTERSON MN; BELL MV; BLOOMFIELD J; DAVIES KE MOLECULAR ANALYSIS OF THE FRAGILE-X SYNDROME | 1 | 1 |
| 1606 | 0 | 0 | 614 1988 ZEITSCHRIFT FUR KLINISCHE MEDIZIN-ZKM 43(6):451-454 STEINBICKER V; SEEMANOVA E; MISSBACH D THE SYNDROME OF THE FRAGILE X (MARTIN-BELL-SYNDROME MBS) | 0 | 1 |
| 1607 | 0 | 0 | 615 1989 AMERICAN FAMILY PHYSICIAN 39(5):185-193 SIMENSEN RJ; ROGERS RC FRAGILE-X SYNDROME | 1 | 1 |
| 1608 | 2 | 10 | 637 1989 CYTOGENETICS AND CELL GENETICS 50(2-3):172-173 SAUER SM; PHELAN MC; RICHER CL; SCHWARTZ CE PHYSICAL MAPPING OF PROBES PROXIMAL TO THE FRAGILE-X LOCUS (FRAX) CONFIRMS THE ORDER F9-DXS105 (CX55.7)-DXS98 (4D8)-FRAXA | 1 | 1 |
| 1609 | 0 | 0 | 639 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1007-1007 GOONEWARDENA P; GROSS AC; FERRANDO CJ; BROWN T; DAHL N; et al. ANONYMOUS DNA PROBE U6.2 (DXS304) FROM XQ MAPS DISTAL TO THE DXS98 LOCUS AND SHOWS CLOSE LINKAGE TO THE FRAGILE-X SYNDROME | 0 | 1 |
| 1610 | 0 | 0 | 640 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1009-1009 GROSS AC; FERRANDO CJ; BROWN WT LINKAGE DATA FOR FRAGILE-X AND 3 DISTAL MARKERS | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1611 | 0 | 0 | 642 1989 CYTOGENETICS AND CELL GENETICS 51(1-4):1089-1090 THIBODEAU SN; SCHAID D; BREN G; BLOOMFIELD J; BELL MV; et al. GENETIC-MAPPING OF A NOVEL REGION CLOSE TO THE FRAGILE X-SITE ON THE HUMAN X-CHROMOSOME | 0 | 1 |
| 1612 | 0 | 0 | 662 1989 NEUROLOGIC CLINICS 7(1):107-121 BROWN WT THE FRAGILE-X SYNDROME | 1 | 1 |
| 1613 | 21 | 41 | 667 1989 PSYCHOLOGY IN THE SCHOOLS 26(4):380-389 SIMENSEN RJ; ROGERS RC SCHOOL-PSYCHOLOGY AND MEDICAL DIAGNOSIS - THE FRAGILE X-SYNDROME | 1 | 1 |
| 1614 | 2 | 3 | 671 1989 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 17(2):85-90 BLANK R MAIN SYMPTOMS - DELAYED LANGUAGE-DEVELOPMENT AND BEHAVIOR PROBLEMS - 2 CASE-REPORTS ON THE FRAGILE-X SYNDROME | 1 | 1 |
| 1615 | 6 | 13 | 699 1990 BRITISH JOURNAL OF HOSPITAL MEDICINE 43(1):17-17 BUNDEY S FRAGILE-X SYNDROME | 1 | 1 |
| 1616 | 1 | 4 | 720 1990 JOURNAL OF NEUROLOGY 237(1):65-66 MUSUMECI SA; FERRI R; BERGONZI P THE SPECIFICITY OF THE CHARACTERISTIC SLEEP EEG PATTERN IN THE FRAGILE-X SYNDROME | 1 | 1 |
| 1617 | 2 | 3 | 736 1990 PRENATAL DIAGNOSIS 10(8):545-546 OOSTRA BA; SANDKUYL LA; HALLEY DJJ RISK CALCULATION OF MISSED PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 1 | 1 |
| 1618 | 0 | 0 | 761 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):231-231 SHAPIRO LR; WILMOT PL PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE X-SYNDROME - DETERMINATION OF ACCURACY | 1 | 1 |
| 1619 | 0 | 0 | 788 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):173-185 SPANO LM; OPITZ JM BIBLIOGRAPHY ON X-LINKED MENTAL-RETARDATION, THE FRAGILE-X, AND RELATED SUBJECTS .5. (1991) | 0 | 1 |
| 1620 | 1 | 8 | 794 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):288-289 ZHAO Y; SHEN Y; LIU Y; ZHANG JC; YE LZ; et al. FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) IN CHINA | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1621 | 7 | 20 | 798 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):311-318 CARPENTER NJ DNA LINKAGE ANALYSIS OF 26 FAMILIES WITH FRAGILE-X SYNDROME | 1 | 1 |
| 1622 | 14 | 31 | 800 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):322-327 GOONEWARDENA P; BROWN WT; GROSS AC; FERRANDO C; DOBKIN C; et al. LINKAGE ANALYSIS OF THE FRAGILE-X SYNDROME USING A NEW DNA MARKER U6.2 DEFINING LOCUS DXS304 | 1 | 1 |
| 1623 | 13 | 23 | 807 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):370-373 BROOKS SS; COHEN I; FERRANDO C; JENKINS EC; BROWN WT; et al. CYTOGENETICALLY NEGATIVE, LINKAGE POSITIVE FRAGILE-X SYNDROME | 0 | 1 |
| 1624 | 1 | 7 | 816 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):416-417 JENKINS LS; GRUENERT DC; JENKINS EC; SCHONBERG SA TRANSFORMATION AND ESTABLISHMENT OF FRAGILE-X CELL-LINES FROM AMNIOCYTES | 1 | 1 |
| 1625 | 2 | 33 | 823 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):456-463 KRAWCZUN MS; JENKINS EC; DUNCAN CJ; STARKHOUCK SL; KUNAPORN S; et al. DISTRIBUTION OF AUTOSOMAL FRAGILE SITES IN SPECIMENS CULTURED FOR PRENATAL FRAGILE-X DIAGNOSIS | 1 | 1 |
| 1626 | 1 | 8 | 824 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):464-466 JENKINS EC; BROOKS SE; STARKHOUCK SL; DUNCAN CJ; BROOKS SLS; et al. SV40-TRANSFORMED FRAGILE(X) AMNIOCYTES | 1 | 1 |
| 1627 | 16 | 38 | 842 1991 BIOESSAYS 13(5):243-251 JORDAN BR FRAGILE X-LINKED MENTAL-RETARDATION AND THE DIFFICULTIES OF REVERSE GENETICS | 1 | 1 |
| 1628 | 5 | 13 | 843 1991 BIOLOGICAL PSYCHIATRY 29(3):298-299 MENDLEWICZ J; HIRSCH D BIPOLAR MANIC-DEPRESSIVE ILLNESS AND THE FRAGILE-X SYNDROME | 0 | 1 |
| 1629 | 4 | 13 | 850 1991 CLINICAL PEDIATRICS 30(5):318-321 HO HH; EAVES LC; PAYNE E VARIABILITY OF DEVELOPMENT IN 3 SIBLINGS WITH FRAGILE-X SYNDROME | 0 | 1 |
| 1630 | 0 | 0 | 855 1991 CYTOGENETICS AND CELL GENETICS 56(3-4):221-221 SHAPIRO LR; EALLONARDO SJ; WILMOT PL INTERNAL CONTROL FOR SUCCESSFUL INDUCTION OF THE FRAGILE X-CHROMOSOME - OTHER FOLATE SENSITIVE FRAGILE SITE EXPRESSION ELIMINATED | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1631 | 2 | 9 | 856 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2054-2055 BOUVET A; BASRUR PK A MARKER FRAGILE X-CHROMOSOME ASSOCIATED WITH BALDY CALF SYNDROME | 1 | 1 |
| 1632 | 6 | 9 | 876 1991 JOURNAL OF MEDICAL GENETICS 28(12):811-813 CONNOR JM CLONING OF THE GENE FOR THE FRAGILE-X SYNDROME - IMPLICATIONS FOR THE CLINICAL GENETICIST | 1 | 1 |
| 1633 | 1 | 6 | 881 1991 JOURNAL OF MEDICAL GENETICS 28(12):837-839 GRIFFITHS MJ; STRACHAN MC A SINGLE LYMPHOCYTE CULTURE FOR FRAGILE-X INDUCTION AND PROMETAPHASE CHROMOSOME ANALYSIS | 0 | 1 |
| 1634 | 8 | 14 | 912 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 42(2):184-186 FINUCANE BM; JAEGER E; DUNN E; SCOTT CI STUDY OF COLOR-VISION IN FRAGILE-X SYNDROME | 1 | 1 |
| 1635 | 8 | 19 | 913 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 42(6):835-838 RAMOS FJ; EMANUEL BS; SPINNER NB FREQUENCY OF THE COMMON FRAGILE SITE AT XQ27.2 UNDER CONDITIONS OF THYMIDYLATE STRESS - IMPLICATIONS FOR CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X SYNDROME | 0 | 1 |
| 1636 | 10 | 14 | 929 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):136-141 JENKINS EC; GENOVESE MJ; DUNCAN CJ; GU H; STARKHOUCK SL; et al. FRA(X)(Q27.2), THE COMMON FRAGILE SITE, OBSERVED IN ONLY ONE OF 760 CASES STUDIED FOR THE FRAGILE-X SYNDROME | 1 | 1 |
| 1637 | 11 | 21 | 930 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):142-148 FISCH GS; FRYNS JP FACTORS WHICH CONTRIBUTE TO CYTOGENETIC FREQUENCY OF EXPRESSION IN FAMILIES OF FRAGILE-X FEMALES | 1 | 1 |
| 1638 | 12 | 19 | 931 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):155-160 JENKINS EC; DUNCAN CJ; GU H; GENOVESE M; KRAWCZUN MS DIALYZED FETAL BOVINE SERUM INCREASES CYTOGENETIC FRAGILE-X EXPRESSION | 1 | 1 |
| 1639 | 4 | 6 | 935 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):170-173 SHAPIRO LR; WILMOT PL; FISCH GS PRENATAL CYTOGENETIC DIAGNOSIS OF THE FRAGILE-X SYNDROME IN AMNIOTIC-FLUID - CALCULATION OF ACCURACY | 1 | 1 |
| 1640 | 11 | 12 | 937 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):181-186 MURPHY PD; WILMOT PL; SHAPIRO LR PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME - RESULTS FROM PARALLEL MOLECULAR AND CYTOGENETIC STUDIES | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1641 | 7 | 22 | 951 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):312-319 CARPENTER NJ; SWARTZBOYD J; PRICHARD JK; LAM T LINKAGE AND RISK ASSESSMENT IN FRAGILE-X FAMILIES USING NEW DNA PROBES AT XQ27 | 1 | 1 |
| 1642 | 5 | 5 | 955 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):339-344 VIANNAMORGANTE AM; OTTO PA NOTES ON THE POPULATION-GENETICS OF FRAGILE X SYNDROME | 1 | 1 |
| 1643 | 1 | 12 | 958 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):505-509 CIANCHETTI C; SANNIOFANCELLO G; FRATTA AL; PISCHEDDA MP; SPINICCI G; et al. NEUROPSYCHOLOGICAL STUDIES IN FAMILIES WITH FRAGILE-X NEGATIVE X-LINKED MENTAL-RETARDATION | 0 | 1 |
| 1644 | 3 | 4 | 971 1992 ARCHIVES FRANCAISES DE PEDIATRIE 49(5):477-477 DROUIN V; VANNIER JP; MOIROT H; MITROFANOFF P; TRON P WILMS-TUMOR AND FRAGILE-X SYNDROME | 1 | 1 |
| 1645 | 5 | 11 | 975 1992 BRITISH MEDICAL JOURNAL 305(6847):208-208 MOORE DWY NEW DEVELOPMENTS IN THE FRAGILE-X SYNDROME | 1 | 1 |
| 1646 | 16 | 24 | 983 1992 DISEASE MARKERS 10(1):1-5 KNIGHT SJL; HIRST MC; DAVIES KE MOLECULAR ANALYSIS OF THE FRAGILE X-SYNDROME | 0 | 1 |
| 1647 | 16 | 33 | 984 1992 EDUCATIONAL RESEARCH 34(3):221-228 GIBB C THE MOST COMMON-CAUSE OF LEARNING-DIFFICULTIES - A PROFILE OF FRAGILE-X SYNDROME AND ITS IMPLICATIONS FOR EDUCATION | 1 | 1 |
| 1648 | 0 | 3 | 996 1992 JAPANESE JOURNAL OF HUMAN GENETICS 37(3):235-239 NATORI N A CASE OF ATYPICAL DUCHENNE TYPE MUSCULAR-DYSTROPHY WITH FRAGILE-X | 0 | 1 |
| 1649 | 7 | 8 | 1002 1992 JOURNAL OF MEDICAL GENETICS 29(10):726-729 TARLETON J; WONG S; HEITZ D; SCHWARTZ C DIFFICULT DIAGNOSIS OF THE FRAGILE X-SYNDROME MADE POSSIBLE BY DIRECT DETECTION OF DNA MUTATIONS | 1 | 1 |
| 1650 | 19 | 25 | 1005 1992 JOURNAL OF PEDIATRICS 121(3):385-390 POTTER NT; LOZZIO CB; ANDERSON IJ; BOWLIN ES; MATTESON KJ USE OF A MOLECULAR GENETIC APPROACH TO DIAGNOSING THE FRAGILE-X GENOTYPE | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1651 | 17 | 25 | 1011 1992 MEDICINA CLINICA 98(4):121-124 GINE R; ESPINAS ML; ANTICH J; CARBALLO M MOLECULAR-GENETICS OF THE FRAGILE-X SYNDROME - MOLECULAR DIAGNOSIS BY DNA PROBES | 1 | 1 |
| 1652 | 19 | 26 | 1028 1992 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 20(2):113-120 VONGONTARD A; HILLIG U; HEROLD D CLINICAL AND CYTOGENETIC PROBLEMS IN THE DIAGNOSIS OF THE FRAGILE-X SYNDROME | 1 | 1 |
| 1653 | 4 | 9 | 1029 1992 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 92(4):28-31 LASTOCHKINA NA; KUPRIYANOVA TA; PUCHINSKAYA LM; MARINCHEVA GS; GORKOVA SA THE CLINICOELECTROPHYSIOLOGICAL CHARACTERIZATION OF WOMEN, HETEROZYGOUS CARRIERS OF FRAGILE X-CHROMOSOME | 1 | 1 |
| 1654 | 0 | 0 | 1040 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):78-78 ROUSSEAU F; HEITZ D; TARLETON J; MACPHERSON J; PETTERSON U; et al. A COLLABORATIVE MULTICENTER STUDY OF DIRECT DIAGNOSIS OF THE FRAGILE-X SYNDROME WITH PROBE STB12.3 - THE 1ST 2253 CASES | 1 | 1 |
| 1655 | 0 | 0 | 1043 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):144-144 HAGERMAN R; HULL C; CARPENTER I; STALEY L; OCONNOR R; et al. HIGH-FUNCTIONING FRAGILE X MALES | 1 | 1 |
| 1656 | 0 | 0 | 1047 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):448-448 HOLDEN JJA; CHALIFOUX M; WING M; WHITE BN; GLOVER T; et al. THE FRAGILE-X SYNDROME AND PREMATURE MENOPAUSE | 1 | 1 |
| 1657 | 0 | 0 | 1051 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):717-717 PERGOLIZZI RG; ERSTER SH; MILLAN CA; GUZOWSKI DE; SELLATI LM STABILITY OF THE CGG REPEAT REGION OF FMR-1 | 1 | 1 |
| 1658 | 0 | 0 | 1082 1993 ANNALES DE PEDIATRIE 40(9):565-572 BLANC DS; DANGELO J; ETANGS NLD AUTISM AND THE FRAGILE X-SYNDROME | 1 | 1 |
| 1659 | 11 | 29 | 1111 1993 HUMAN GENETICS 92(4):373-378 MORNET E; BOGYO A; DELUCHAT C; SIMONBOUY B; MATHIEU M; et al. MOLECULAR ANALYSIS OF A RING CHROMOSOME-X IN A FAMILY WITH FRAGILE-X SYNDROME | 0 | 1 |
| 1660 | 0 | 0 | 1120 1993 IRISH MEDICAL JOURNAL 86(3):92-& KEENAN E; KEANE V; RAMSEY L FRAGILE-X SYNDROME - A REVIEW | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1661 | 10 | 11 | 1132 1993 JOURNAL OF MEDICAL GENETICS 30(3):193-197 KNOBLOCH O; PELZ F; WICK U; NELSON DL; ZOLL B DIRECT VERSUS INDIRECT MOLECULAR DIAGNOSIS OF FRAGILE-X MENTAL-RETARDATION IN 40 GERMAN FAMILIES AT RISK | 1 | 1 |
| 1662 | 6 | 7 | 1143 1993 LANCET 342(8878):1004-1005 YOUNG ID DIAGNOSING FRAGILE-X SYNDROME | 1 | 1 |
| 1663 | 23 | 46 | 1164 1993 PSYCHIATRIE DE L ENFANT 36(1):5-26 LIDAPULIK H; BASQUIN M COGNITIVE DISTURBANCES AND PSYCHIATRIC MANIFESTATIONS IN THE FRAGILE-X SYNDROME - AUTISM AND FRAGILE-X SYNDROME | 0 | 1 |
| 1664 | 3 | 22 | 1168 1993 YOUNG CHILDREN 49(1):73-77 MAZZOCCO MMM; OCONNOR R FRAGILE-X SYNDROME - A GUIDE FOR TEACHERS OF YOUNG-CHILDREN | 0 | 1 |
| 1665 | 3 | 6 | 1185 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):374-377 STEYAERT J; BORGHGRAEF M; FRYNS JP APPARENTLY ENHANCED VISUAL INFORMATION-PROCESSING IN FEMALE FRAGILE-X CARRIERS - PRELIMINARY FINDINGS | 1 | 1 |
| 1666 | 5 | 8 | 1193 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):436-442 JENKINS EC; MORYS I; HENDERSON J; GENOVESE M; CARTER M; et al. FRAGILE-X INDUCTION SYSTEMS IN CVS CULTURES - EFFECT ON CYTOGENETIC, PCR, AND GENOMIC SOUTHERN BLOT DNA ANALYSES OF THE FMR-1 GENE | 1 | 1 |
| 1667 | 7 | 8 | 1197 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):452-453 JENKINS EC; GENOVESE M; DUNCAN CJ; GU H; STARKHOUCK S; et al. OCCURRENCE OF ANEUPLOIDY FOR THE X-CHROMOSOME IN OVER 1,300 UNRELATED SPECIMENS SCREENED FOR THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 1668 | 10 | 11 | 1223 1994 ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE 148(1):63-64 LEUNG AKC; MCLEOD DR; ROBSON WLM; FAGAN JE PICTURE OF THE MONTH - FRAGILE-X SYNDROME | 0 | 1 |
| 1669 | 14 | 28 | 1224 1994 BRITISH JOURNAL OF CLINICAL PRACTICE 48(1):42-44 PATEL BD THE FRAGILE-X SYNDROME | 1 | 1 |
| 1670 | 0 | 0 | 1225 1994 CANADIAN FAMILY PHYSICIAN 40:290-295 WIEBE E; WIEBE A FRAGILE-X SYNDROME | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1671 | 6 | 7 | 1231 1994 CLINICAL GENETICS 45(4):186-189 LOPEZPAJARES I; DELICADO A; PASCUALCASTROVIEJO I; LOPEZMARTIN V; MORENO F; et al. FRAGILE-X SYNDROME WITH EXTRA MICROCHROMOSOME | 0 | 1 |
| 1672 | 1 | 1 | 1249 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(1):28-28 BROWN WT; HOUCK GE; JEZIOROWSKA A; LEVINSON FN; DING X; et al. RAPID FRAGILE-X CARRIER SCREENING AND PRENATAL-DIAGNOSIS USING A NONRADIOACTIVE PCR TEST (VOL 270, PG 1569, 1993) | 1 | 1 |
| 1673 | 6 | 12 | 1264 1994 JOURNAL OF MEDICAL GENETICS 31(12):950-952 CURTIS G; DENNIS N; MACPHERSON J THE IMPACT OF GENETIC-COUNSELING ON FEMALES IN FRAGILE-X FAMILIES | 1 | 1 |
| 1674 | 2 | 2 | 1271 1994 MENTAL RETARDATION 32(2):156-156 SPITZ HH FRAGILE-X SYNDROME IS NOT THE 2ND LEADING CAUSE OF MENTAL-RETARDATION | 0 | 1 |
| 1675 | 0 | 0 | 1279 1994 PEDIATRIC RESEARCH 35(4):A23-A23 LACHIEWICZ AM; DAWSON DV AUTISTIC BEHAVIORS OF YOUNG GIRLS WITH FRAGILE X-SYNDROME | 1 | 1 |
| 1676 | 10 | 22 | 1362 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):223-229 King RA; Hagerman R; Houghton M Ocular findings in fragile X syndrome | 1 | 1 |
| 1677 | 27 | 36 | 1363 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):230-241 Brun C; Obiols JE; Cheema A; OConnor R; Riddle J; et al. Longitudinal IQ changes in fragile X females | 1 | 1 |
| 1678 | 26 | 41 | 1368 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):293-301 Jenkins EC; Houck GE; Ding XH; Li SY; StarkHouck SL; et al. An update on fragile X prenatal diagnosis: End of the cytogenetic testing era | 1 | 1 |
| 1679 | 0 | 0 | 1377 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):390-395 McConkieRosell A; Robinson H; Wake S; Staley L; Heller K; et al. Educating extended family members about the inheritance of the fragile X syndrome | 0 | 1 |
| 1680 | 0 | 5 | 1394 1995 HUMAN GENETICS 96(3):369-370 LENCH NJ; THOMPSON J; MARKHAM AF; ROBINSON PA (CGG) TRINUCLEOTIDE REPEAT POLYMORPHISM IN THE 5'-REGION OF THE HHR6B GENE - THE HUMAN HOMOLOG OF THE YEAST DNA-REPAIR GENE RAD6 | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1681 | 8 | 11 | 1399 1995 ISRAEL JOURNAL OF MEDICAL SCIENCES 31(5):323-325 DAR H; SCHAAP T; BAITOR H; BOROCHOWITZ Z; GELMANKOHAN Z; et al. ETHNIC DISTRIBUTION OF THE FRAGILE-X SYNDROME IN ISRAEL - EVIDENCE OF FOUNDER CHROMOSOMES() | 1 | 1 |
| 1682 | 5 | 24 | 1400 1995 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 25(6):655-662 Lenti C; Peruzzi C; Bianchini E The association between autism and fragile X syndrome: A case report | 0 | 1 |
| 1683 | 15 | 26 | 1410 1995 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 39:544-553 Butler MG; Pratesi R; VnencakJones CL Molecular genetic analysis of mentally retarded males with features of the fragile-X syndrome | 0 | 1 |
| 1684 | 9 | 21 | 1438 1995 PSYCHIATRIC GENETICS 5(4):157-160 Jonsson E; Bjorck E; Wahlstrom J; Gustavsson P; Sedvall G Screening for CGG trinucleotide repeat expansion in the fragile X mental retardation 1 gene in schizophrenic patients | 0 | 1 |
| 1685 | 11 | 24 | 1446 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 63(2):396-400 Giampietro PF; Haas BR; Lipper E; Gutman A; Zellers NJ; et al. Fragile X syndrome in two siblings with major congenital malformations | 0 | 1 |
| 1686 | 11 | 21 | 1522 1996 CLINICAL OBSTETRICS AND GYNECOLOGY 39(4):772-782 Finucane B Should all pregnant women be offered carrier testing for fragile X syndrome? | 1 | 1 |
| 1687 | 1 | 4 | 1557 1996 JOURNAL OF SLEEP RESEARCH 5(4):272-272 Musumeci SA; Ferri R; Elia M; DelGracco S; Scuderi C; et al. Normal respiratory pattern during sleep in young fragile X-syndrome patients | 1 | 1 |
| 1688 | 9 | 33 | 1558 1996 KOREAN JOURNAL OF GENETICS 18(3):199-210 Choi SK; Kim HY; Paik YK Cytogenetic analysis of a Korean family with fragile X syndrome | 0 | 1 |
| 1689 | 13 | 45 | 1565 1996 NIMHANS JOURNAL 14(3):201-207 Suresh KP; Girimaji SR; Manjunatha KR Newer genetics in mental retardation .1. Fragile X syndrome and triplet repeat mutations | 0 | 1 |
| 1690 | 0 | 0 | 1594 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A30-A30 Gunter C; Paradee W; Newman J; Sherman SL; Warren ST A novel biallelic polymorphism in the FMR1 gene shows strong linkage disequilibrium With CGG repeats and flanking microsatellite markers. | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1691 | 0 | 0 | 1610 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A306-A306 Chiurazzi P; Pomponi MG; Willemsen R; Oostra BA; Neri G In vitro reactivation of the fragile X syndrome gene. | 1 | 1 |
| 1692 | 0 | 0 | 1613 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A321-A321 Tassone F; Hagerman RJ; Ikle D; Dyer PN; Lampe M; et al. FMRP expression as a potential prognostic indicator in fragile X syndrome. | 1 | 1 |
| 1693 | 51 | 134 | 1670 1997 INTERNATIONAL REVIEW OF RESEARCH IN MENTAL RETARDATION, VOL 21 21:221-247 Fisch GS Longitudinal assessment of cognitive-behavioral deficits produced by the fragile-X mutation | 0 | 1 |
| 1694 | 1 | 2 | 1683 1997 JOURNAL OF MEDICAL GENETICS 34(4):350-350 Loesch DZ FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male | 1 | 1 |
| 1695 | 3 | 10 | 1702 1997 PEDIATRICS 99(5):753-753 Hagerman R Fragile X: Treatment of hyperactivity | 0 | 1 |
| 1696 | 31 | 49 | 1708 1997 REVISTA DE NEUROLOGIA 25(143):1068-1071 EstevezGonzalez A; Roig C; Piles S; Pineda M; GarciaSanchez C Fragile-X syndrome and mental retardation | 1 | 1 |
| 1697 | 8 | 22 | 1711 1997 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 97(8):33-37 Gorbachevskaya NL; Denisova LV Bioelectric brain activity in patients with syndrome of fragile X-chromosome and in their mothers | 0 | 1 |
| 1698 | 19 | 30 | 1728 1998 CLINICAL GENETICS 54(4):309-314 Russo S; Briscioli V; Cogliati F; Macchi M; Lalatta F; et al. An unusual fragile X sibship: female compound heterozygote and male with a partially methylated full mutation | 0 | 1 |
| 1699 | 0 | 10 | 1744 1998 GENERAL HOSPITAL PSYCHIATRY 20(2):126-127 Silva JA; Ferrari MM; Leong GB Erotomania in a case of fragile-X syndrome | 0 | 1 |
| 1700 | 4 | 7 | 1747 1998 HUMAN GENETICS 102(1):54-56 Storm K; Handig I; Reyniers E; Oostra BA; Kooy RF; et al. Incomplete EcoRI digestion may lead to false diagnosis of fragile X syndrome | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1701 | 0 | 0 | 1755 1998 HUMAN MUTATION 12(6):432-432 Wang YC; Li SY Point mutation in intron 10 of FMR1 is unlikely to be a cause of fragile X syndrome - Response | 0 | 1 |
| 1702 | 17 | 40 | 1784 1998 JOURNAL OF NEUROSCIENCE RESEARCH 51(1):41-48 Berry-Kravis E; Ciurlionis R Overexpression of fragile X gene (FMR-1) transcripts increases cAMP production in neural cells | 1 | 1 |
| 1703 | 30 | 41 | 1795 1998 REVISTA MEDICA DE CHILE 126(8):911-918 Jara L; Lopez M; Mellado C; Aspillaga M; Avendano I; et al. Clinical and metabolic screening for fragile X syndrome in 300 patients with unspecific mental retardation | 1 | 1 |
| 1704 | 10 | 25 | 1796 1998 REVISTA MEDICA DE CHILE 126(12):1447-1454 Aspillaga M; Jara L; Avendano I; Lopez M Fragile X syndrome. Clinical analysis of 300 Chilean patients with unspecific mental retardation | 1 | 1 |
| 1705 | 0 | 0 | 1816 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A403-A403 Xu B; School JM; Buroker NE; Scott CR; Chen SH High frequency of the FMR-1 INV10+14c/t polymorphism in Asians, and its association with the Fragile X Syndrome in Caucasians. | 0 | 1 |
| 1706 | 11 | 22 | 1836 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):318-321 Linden MG; Tassone F; Gane LW; Hills JL; Hagerman RJ; et al. Compound heterozygous female with fragile X syndrome | 0 | 1 |
| 1707 | 18 | 22 | 1855 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):229-232 Petek E; Kroisel PM; Schuster M; Zierler H; Wagner K Mosaicism in a fragile X male including a de novo deletion in the FMR1 gene | 1 | 1 |
| 1708 | 5 | 13 | 1864 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 85(3):197-201 Freedenberg DL; Gane LW; Richards CS; Lampe M; Hills J; et al. Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal development | 1 | 1 |
| 1709 | 10 | 14 | 1865 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 85(3):311-316 Grasso M; Faravelli F; Lo Nigro C; Chiurazzi P; Sperandeo MP; et al. Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients | 1 | 1 |
| 1710 | 17 | 24 | 1870 1999 AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 181(4):789-792 Wenstrom KD; Descartes M; Franklin J; Cliver SP A five-year experience with fragile X screening of high-risk gravid women | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1711 | 0 | 0 | 1873 1999 ARCHIVES OF CLINICAL NEUROPSYCHOLOGY 14(8):767-768 Lanham DC; Mazzocco MM; Denckla MB Depression and anxiety in girls with Fragile X or Turner Syndrome. | 1 | 1 |
| 1712 | 6 | 10 | 1897 1999 HEREDITAS 130(2):189-190 Sucharov CC; Silva R; Rondinelli E; Moura-Neto RS Fragile X trinucleotide repeats from a normal population in Rio de Janeiro, Brazil | 0 | 1 |
| 1713 | 0 | 0 | 1904 1999 HUMAN REPRODUCTION 14:354-355 Gersak K; Kregar-Velikonja N; Meden-Vrtovec H; Peterlin B Fragile X premutation screening in women with premature menopause | 1 | 1 |
| 1714 | 9 | 29 | 1905 1999 INTERNATIONAL JOURNAL OF BEHAVIORAL DEVELOPMENT 23(2):519-531 Burack JA; Shulman C; Katzir E; Schaap T; Brennan JM; et al. Cognitive and behavioural development of Israeli males with fragile X and Down Syndrome | 1 | 1 |
| 1715 | 7 | 18 | 1908 1999 JOURNAL OF CHILD NEUROLOGY 14(2):108-112 Singh R; Sutherland GR; Manson J Partial seizures with focal epileptogenic electroencephalographic patterns in three related female patients with fragile-X syndrome | 1 | 1 |
| 1716 | 10 | 21 | 1915 1999 JOURNAL OF MEDICAL GENETICS 36(2):167-170 de Vries BBA; van den Boer-van den Berg HMA; Niermeijer MF; Tibben A Dilemmas in Counselling females with the fragile X syndrome | 0 | 1 |
| 1717 | 10 | 20 | 1934 1999 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 27(3):175-181 Sarimski K Play and communicative behaviour in young boys with fragile-X syndrome. | 0 | 1 |
| 1718 | 0 | 0 | 1943 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):18-18 Brown V; Ceman S; Jin P; Jin C; Wilkinson KD; et al. Messenger RNAs associated with the fragile X mental retardation protein in mouse brain. | 1 | 1 |
| 1719 | 0 | 0 | 1959 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):360-360 Ramos FJ; Mila M; Ortilles M; Rife M; Tazon B; et al. Validity of the analysis of the FMRP expression in bloodsmears as a screening method for the Fragile X Syndrome. | 1 | 1 |
| 1720 | 0 | 0 | 1963 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):366-366 Raca G; Siyanova E; Mirkin S Janus effects of premutation size CGG repeats on gene expression. | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1721 | 11 | 16 | 2013 2000 GENETIC TESTING 4(3):235-239 Tzountzouris J; Kennedy D; Skuterud M; Connolly-Wilson M; Holden JJA; et al. Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: Implications for molecular diagnosis of the Fragile X syndrome | 0 | 1 |
| 1722 | 6 | 10 | 2014 2000 GENETIC TESTING 4(3):241-242 Brown WT; Nolin SL Apparent FMR1 allele instability in non-Fragile X males - Invited commentary | 0 | 1 |
| 1723 | 1 | 2 | 2028 2000 HUMAN REPRODUCTION 15(8):1874-1875 Marozzi A Regarding recall bias in the association between idiopathic premature ovarian failure and fragile X premutation | 1 | 1 |
| 1724 | 0 | 0 | 2046 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:317-317 Karrer JH; Hagerman RJ; Karrer RS; Fitzpatrick D; Vavold J; et al. Genotypic-specific event-related brain potentials among infants and toddlers with fragile-X syndrome and Down syndrome | 1 | 1 |
| 1725 | 4 | 15 | 2066 2000 JOURNAL OF PSYCHOEDUCATIONAL ASSESSMENT 18(3):255-267 Hooper SR; Hatton DD; Baranek GT; Roberts JP; Bailey DB Nonverbal assessment of IQ, attention, and memory abilities in children with fragile-X syndrome using the Leiter-R | 1 | 1 |
| 1726 | 28 | 43 | 2078 2000 MOLECULAR DIAGNOSIS 5(3):169-178 Gold B; Radu D; Balanko A; Chiang CS Diagnosis of Fragile X syndrome by Southern blot hybridization using a chemiluminescent probe: A laboratory protocol | 0 | 1 |
| 1727 | 3 | 6 | 2090 2000 PRENATAL DIAGNOSIS 20(10):854-855 Wilkin H; Tuohy J; Theewis W Prenatal diagnosis of fragile X and Turner mosaicism in a 12-week fetus | 1 | 1 |
| 1728 | 1 | 10 | 2092 2000 VETERINARNI MEDICINA 45(10-11):308-310 Slota E; Danielak-Czech B; Pietraszewska J; Kozubska-Sobocinska A Preliminary identification of the fragile X in two crossbred cows | 0 | 1 |
| 1729 | 4 | 7 | 2114 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 100(2):156-161 Kjaer I; Hjalgrim H; Russell BG Cranial and hand skeleton in fragile X syndrome | 0 | 1 |
| 1730 | 35 | 62 | 2133 2001 BRAIN RESEARCH BULLETIN 56(3-4):383-387 Chiurazzi P; Neri G Pharmacological reactivation of inactive genes: The fragile X experience | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1731 | 65 | 94 | 2142 2001 CURRENT OPINION IN PSYCHIATRY 14(5):443-449 Eliez S; Feinstein C The fragile X syndrome: bridging the gap from gene to behavior | 0 | 1 |
| 1732 | 4 | 6 | 2151 2001 GENETIC TESTING 5(2):139-140 Gilbert F Comment: How many are too many when discussing triplet repeats in the FMR1 gene and the fragile X syndrome? | 0 | 1 |
| 1733 | 6 | 47 | 2191 2001 NUCLEIC ACIDS RESEARCH 29(22):4684-4690 Fojtik P; Vorlickova M The fragile X chromosome (GCC) repeat folds into a DNA tetraplex at neutral pH | 0 | 1 |
| 1734 | 9 | 15 | 2201 2001 REVISTA DE NEUROLOGIA 33:S29-S32 Brun-Gasca C; Artigas-Pallares J Psycholinguistic aspects of fragile X chromosome syndrome | 0 | 1 |
| 1735 | 0 | 0 | 2212 2001 SCIENCE 294(5548):1809-1809 Sohn E Genetics - Fragile X's missing partners identified | 0 | 1 |
| 1736 | 16 | 28 | 2216 2002 ACTA PAEDIATRICA 91(5):535-539 Hecimovic S; Tarnik IP; Baric I; Cakarun Z; Pavelic K Screening for fragile X syndrome: results from a school for mentally retarded children | 1 | 1 |
| 1737 | 0 | 0 | 2230 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):507-507 Neri G; Tabolacci E; Pietrobono R; Pomponi MG; Chiurazzi P Histone hyperacetylation and reactivation of the fragile X syndrome gene. | 0 | 1 |
| 1738 | 6 | 7 | 2235 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 107(4):344-345 Vink GR; Froster UG Comparison of FMR1-protein expression in lymphocytes, methylation pattern in Southern blot analysis, and IQ values in three sisters with the fragile X syndrome | 1 | 1 |
| 1739 | 8 | 44 | 2245 2002 AMERICAN JOURNAL OF OCCUPATIONAL THERAPY 56(5):538-546 Baranek GT; Chin YKH; Hess LMG; Yankee JG; Hatton DD; et al. Sensory processing correlates of occupational performance in children with fragile X syndrome: Preliminary findings | 1 | 1 |
| 1740 | 13 | 35 | 2249 2002 ARCHIVES OF MEDICAL RESEARCH 33(2):128-135 Wang TS; Hsieh LJ; Hsu TY; Chung CH; Li SY DNA damage and repair in lymphoblastoid cell lines from normal donors and fragile X syndrome patients | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1741 | 4 | 53 | 2295 2002 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 43(7):949-957 von Gontard A; Backes M; Laufersweiler-Plass C; Wendland C; Lehmkuhl G; et al. Psychopathology and familial stress - comparison of boys with Fragile X syndrome and Spinal Muscular Atrophy | 0 | 1 |
| 1742 | 0 | 0 | 2306 2002 JOURNAL OF THE AMERICAN GERIATRICS SOCIETY 50(4):S48-S48 Grigsby J; Leehey M; Hagerman RJ; Epstein J; Wilson R; et al. Dementia and a tremor-ataxia disorder among older male carriers of the fragile X premutation. | 0 | 1 |
| 1743 | 55 | 82 | 2309 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):135-144 Kaufmann WE; Cohen S; Sun HT; Ho G Molecular phenotype of fragile X syndrome: FMRP, FXRPs, and protein targets | 1 | 1 |
| 1744 | 0 | 0 | 2321 2002 MOVEMENT DISORDERS 17:S351-S351 Leehey MA; Grigsby J; Rubinstein D; Jacquemont S; Greco C; et al. Parkinsonism, tremor and ataxia in a female fragile X carrier | 1 | 1 |
| 1745 | 0 | 10 | 2338 2002 PANMINERVA MEDICA 44(1):7-10 Bargagna S; Canepa G; Tinelli F Social adjustment in children with Down mental retardation (MRD) and Fragile-X mental retardation (MRX) | 0 | 1 |
| 1746 | 12 | 22 | 2381 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 122A(2):108-114 Heine-Suner D; Torres-Juan L; Morla M; Busquets X; Barcelo F; et al. Fragile-X syndrome and skewed X-chromosome inactivation within a family: A female member with complete inactivation of the functional X chromosome | 0 | 1 |
| 1747 | 22 | 50 | 2387 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(6):373-390 Hatton DD; Wheeler AC; Skinner ML; Bailey DB; Sullivan KM; et al. Adaptive behavior in children with fragile X syndrome | 0 | 1 |
| 1748 | 0 | 0 | 2390 2003 ANNALS OF NEUROLOGY 54:S105-S106 Kaufmann WE; Danko CG; Kau ASM; Thevarajah S; Bukelis I; et al. Increased protein acetylation in lymphocytes predicts autistic behavior in Fragile X syndrome | 1 | 1 |
| 1749 | 26 | 36 | 2406 2003 BRAIN RESEARCH 972(1-2):9-15 Segal M; Kreher U; Greenberger V; Braun K Is fragile X mental retardation protein involved in activity-induced plasticity of dendritic spines? | 0 | 1 |
| 1750 | 14 | 24 | 2419 2003 EUROPEAN CHILD & ADOLESCENT PSYCHIATRY 12(4):172-177 Sabaratnam M; Murthy NV; Wijeratne A; Buckingham A; Payne S Autistic-like behaviour profile and psychiatric morbidity in Fragile X Syndrome - A prospective ten-year follow-up study | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1751 | 15 | 55 | 2424 2003 GENETICS IN MEDICINE 5(5):378-384 Skinner D; Sparkman KL; Bailey DB Screening for fragile X syndrome: Parent attitudes and perspectives | 1 | 1 |
| 1752 | 0 | 34 | 2434 2003 INTERNAL MEDICINE 42(1):110-116 Momoi A; Komura Y; Kumon L; Tamai M; Tarumi Y; et al. Mesenteric venous thrombosis in hereditary protein c deficiency with the mutation at Arg169 (CGG -> TGG) | 0 | 1 |
| 1753 | 10 | 57 | 2438 2003 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 24(4):267-275 Johnston C; Hessl D; Blasey C; Eliez S; Erba H; et al. Factors associated with parenting stress in mothers of children with fragile X syndrome | 0 | 1 |
| 1754 | 7 | 32 | 2443 2003 JOURNAL OF INTELLECTUAL & DEVELOPMENTAL DISABILITY 28(2):135-144 Richdale AL A descriptive analysis of sleep behaviour in children with Fragile X | 1 | 1 |
| 1755 | 28 | 41 | 2448 2003 JOURNAL OF MEDICAL GENETICS 40(7):535-539 de Vries BBA; Severijnen LA; Jacobs A; Olmer R; Halley DJJ; et al. FMRP expression studies in blood and hair roots in a fragile X family with methylation mosaics | 1 | 1 |
| 1756 | 2 | 5 | 2453 2003 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 42(5):516-517 Lung FW; Chen PJ Fragile X syndrome in adolescent prostitutes in southern Taiwan | 0 | 1 |
| 1757 | 41 | 101 | 2465 2003 NEUROPSYCHOLOGY 17(4):646-657 Loesch DZ; Bui QM; Grigsby J; Butler E; Epstein J; et al. Effect of the fragile X status categories and the fragile X mental retardation protein levels on executive functioning in males and females with fragile X | 1 | 1 |
| 1758 | 12 | 40 | 2478 2003 YONSEI MEDICAL JOURNAL 44(4):583-592 Demirhan O; Tastemir D; Diler RS; Firat S; Avei A A cytogenetic study in 120 Turkish children with intellectual disability and characteristics of fragile X syndrome | 1 | 1 |
| 1759 | 2 | 10 | 2483 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(4):730-731 Mandel JL Comparative frequency of fragile-X (FMR1) and creatine transporter (SLC6A8) mutations in X-linked mental retardation | 1 | 1 |
| 1760 | 20 | 26 | 2491 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 129A(3):218-224 Biancalana V; Beldjord C; Taillandier A; Szpiro-Tapia S; Cusin V; et al. Five years of molecular diagnosis of Fragile X syndrome(1997-2001): A collaborative study reporting 95% of the activity in France | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1761 | 17 | 51 | 2495 2004 AMERICAN JOURNAL ON MENTAL RETARDATION 109(3):208-218 Philofsky A; Hepburn SL; Hayes A; Hagerman R; Rogers SJ Linguistic and cognitive functioning and autism symptoms in young children with fragile X syndrome | 0 | 1 |
| 1762 | 14 | 79 | 2496 2004 AMERICAN JOURNAL ON MENTAL RETARDATION 109(3):237-254 Abbeduto L; Seltzer MM; Shattuck P; Krauss MW; Orsmond G; et al. Psychological well-being and coping in mothers of youths with autism, Down syndrome, or fragile X syndrome | 0 | 1 |
| 1763 | 14 | 50 | 2498 2004 ARCHIVES OF GENERAL PSYCHIATRY 61(3):281-288 Garrett AS; Menon V; MacKenzie K; Reiss AL Here's looking at you, kid - Neural systems underlying face and gaze processing in fragile X syndrome | 0 | 1 |
| 1764 | 5 | 41 | 2513 2004 DEVELOPMENTAL SCIENCE 7(1):116-130 Scerif G; Cornish K; Wilding J; Driver J; Karmiloff-Smith A Visual search in typically developing toddlers and toddlers with Fragile X or Williams syndrome | 1 | 1 |
| 1765 | 41 | 114 | 2519 2004 GENES BRAIN AND BEHAVIOR 3(6):337-359 Yan QJ; Asafo-Adjei PK; Arnold HM; Brown RE; Bauchwitz RP A phenotypic and molecular characterization of the fmr1-tm1Cgr Fragile X mouse | 1 | 1 |
| 1766 | 15 | 49 | 2524 2004 GENOMICS 83(1):106-118 Naumann F; Remus R; Schmitz B; Doerfler W Gene structure and expression of the 5 '-(CGG)(n)-3 '-binding protein (CGGBP1) | 0 | 1 |
| 1767 | 2 | 6 | 2533 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(24):2945-2946 Hagerman PJ; Hagerman RJ; Gane LW Genetic counseling for families of patients with fragile X syndrome - In reply | 1 | 1 |
| 1768 | 0 | 30 | 2538 2004 JOURNAL OF CLINICAL MICROBIOLOGY 42(8):3538-3548 Otsuka Y; Parniewski P; Zwolska Z; Kai M; Fujino T; et al. Characterization of a trinucleotide repeat sequence (CGG)(5) and potential use in restriction fragment length polymorphism typing of Mycobacterium tuberculosis | 0 | 1 |
| 1769 | 16 | 25 | 2562 2004 JOURNAL OF NEUROSCIENCE 24(47):10579-10583 Gabel LA; Won S; Kawai H; McKinney M; Tartakoff AM; et al. Visual experience regulates transient expression and dendritic localization of Fragile X mental retardation protein | 1 | 1 |
| 1770 | 16 | 48 | 2567 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):3-10 Bailey DB Newborn screening for fragile X syndrome | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1771 | 34 | 67 | 2568 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):11-16 Cornish K; Sudhalter V; Turk J Attention and language in fragile X | 1 | 1 |
| 1772 | 29 | 55 | 2570 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):25-30 Hagerman PJ; Hagerman RJ Fragile X-associated tremor/ataxia syndrome (FXTAS) | 0 | 1 |
| 1773 | 39 | 66 | 2571 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):31-41 Loesch DZ; Huggins RM; Hagerman RJ Phenotypic variation and FMRP levels in fragile X | 1 | 1 |
| 1774 | 19 | 32 | 2573 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):49-52 Darnell JC; Warren ST; Darnell RB The fragile X mental retardation protein, FMRP, recognizes G-quartets | 0 | 1 |
| 1775 | 11 | 11 | 2579 2004 MOLECULAR HUMAN REPRODUCTION 10(10):773-776 Rife M; Badenas C; Quinto L; Puigoriol E; Tazon B; et al. Analysis of CGG variation through 642 meioses in Fragile X families | 1 | 1 |
| 1776 | 11 | 41 | 2581 2004 MOLECULAR PSYCHIATRY 9(4):417-425 Frankland PW; Wang Y; Rosner B; Shimizu T; Balleine BW; et al. Sensorimotor gating abnormalities in young males with fragile X syndrome and Fmr1-knockout mice | 0 | 1 |
| 1777 | 18 | 61 | 2613 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(50):17428-17433 Ling SC; Fahrner PS; Greenough WT; Gelfand VI Transport of Drosophila fragile X rental retardation protein-containing ribonucleoprotein granules by kinesin-1 and cytoplasmic dynein | 0 | 1 |
| 1778 | 16 | 20 | 2623 2005 ANNALS OF NEUROLOGY 57(1):144-147 Berry-Kravis E; Potanos K; Weinberg D; Zhou LL; Goetz CG Fragile X-associated tremor/ataxia syndrome in sisters related to X-inactivation | 0 | 1 |
| 1779 | 10 | 98 | 2624 2005 APPLIED PSYCHOLINGUISTICS 26(1):7-27 Rice ML; Warren SF; Betz SK Language symptoms of developmental language disorders: An overview of autism, Down syndrome, fragile X, specific language impairment, and Williams syndrome | 0 | 1 |
| 1780 | 11 | 56 | 2643 2005 NEURON 45(5):753-764 McBride SMJ; Choi CH; Wang Y; Liebelt D; Braunstein E; et al. Pharmacological rescue of synaptic plasticity, courtship behavior, and mushroom body defects in a Drosophila model of fragile X syndrome | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1781 | 59 | 77 | 2647 2005 TRENDS IN GENETICS 21(1):37-45 Zhang YQ; Broadie K Fathoming fragile X in fruit flies | 1 | 1 |
| 1782 | 0 | 1 | 1 1967 NEW PHYTOLOGIST 66(1):138-& CORNER EJH VANSTEENIS,CGG - PACIFIC PLANT AREAS 2 | 0 | 0 |
| 1783 | 0 | 0 | 2 1976 GASTROENTEROLOGY 70(5):875-875 SILVA LCD; SETTE H; ANTONACIO F; STRASSMAN P; LOPES JD COMMERCIAL GAMMAGLOBULIN (CGG) AS A POSSIBLE VEHICLE OF TRANSMISSION OF HB-S AG IN FAMILIAL CLUSTERING | 0 | 0 |
| 1784 | 0 | 0 | 3 1979 PSYCHOPHYSIOLOGY 16(2):194-195 HOLZL R NON-INVASIVE MEASUREMENT OF GASTRIC-MOTILITY BY CONJOINT GASTROGRAPHY (CGG) - METHOD AND PSYCHO-PHYSIOLOGICAL APPLICATIONS | 0 | 0 |
| 1785 | 0 | 1 | 4 1980 AMERICAN JOURNAL OF HUMAN GENETICS 32(6):A73-A73 JACKY PB EXPRESSION IN FIBROBLAST-CULTURE OF THE FRAGILE X-CHROMOSOME ASSOCIATED WITH FAMILIAL SEX-LINKED MENTAL-RETARDATION - FACTORS INFLUENCING A RELIABLE DETERMINATION OF THE FREQUENCY OF EXPRESSION | 0 | 0 |
| 1786 | 0 | 0 | 13 1981 ANGLO-WELSH REVIEW (68):6-9 WESTLEY M 'FRAGILE-X' | 0 | 0 |
| 1787 | 0 | 0 | 15 1981 CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES 8(2):191-191 SERGOVICH F; POZSONYI J; HINTON G RECENT ADVANCES IN MENTAL-RETARDATION THE FRAGILE X-CHROMOSOME | 1 | 0 |
| 1788 | 0 | 0 | 20 1981 CLINICAL RESEARCH 29(1):A134-A134 HERBST DS; GERRARD JW; DUNN HG; DILL FJ; KALOUSEK DK; et al. NONSPECIFIC X-LINKED MENTAL-RETARDATION, MACRO-ORCHIDISM AND THE FRAGILE X-CHROMOSOME MARKER | 0 | 0 |
| 1789 | 1 | 7 | 32 1981 LYON MEDICAL 246(20):428-429 [Anon] MENTAL-RETARDATION DUE TO A FRAGILE X-CHROMOSOME | 0 | 0 |
| 1790 | 0 | 0 | 34 1981 PEDIATRIC RESEARCH 15(4):560-560 CARPENTER NJ; LEICHTMAN LG; SAY B STUDIES ON THE FRAGILE X-SYNDROME IN SUBJECTS WITH MENTAL-RETARDATION OF UNKNOWN ETIOLOGY | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1791 | 0 | 0 | 54 1982 BEHAVIOR GENETICS 12(6):599-599 THEOBALD TM; HAY DA BEHAVIORAL-CORRELATES OF THE FRAGILE X-SYNDROME | 0 | 0 |
| 1792 | 0 | 0 | 56 1982 CLINICAL RESEARCH 30(2):A291-A291 BROWN WT; JENKINS EC; FRIEDMAN E; WISNIEWSKI K; FRENCH JH THE FRAGILE X-SYNDROME - A GENETIC CAUSE OF AUTISM | 0 | 0 |
| 1793 | 0 | 0 | 58 1982 CLINICAL RESEARCH 30(5):A890-A890 KRUMDIECK CL; HOWARDPEEBLES PN THE ORIGIN OF THE FRAGILE X IN HUMAN-CHROMOSOMES - AN HYPOTHESIS | 0 | 0 |
| 1794 | 0 | 0 | 75 1982 JOURNAL OF MEDICAL GENETICS 19(5):371-371 WILLATT LR; DAVIS J FRAGILE-X MENTAL-RETARDATION IN TWINS - A CASE-HISTORY | 0 | 0 |
| 1795 | 0 | 0 | 91 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A81-A81 BROWN T; JENKINS E; SHAPIRO LR FRAGILE (X) SYNDROME PRENATAL-DIAGNOSIS REGISTRY | 0 | 0 |
| 1796 | 0 | 0 | 94 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A117-A117 SHAPIRO LR; SUMMA GM; WILMOT PL; GLOTH E SCREENING AND DETECTION OF THE FRAGILE X-SYNDROME | 0 | 0 |
| 1797 | 0 | 0 | 98 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A135-A135 HOWARDPEEBLES PN FRAGILE X-CHROMOSOME - TECHNICAL ASPECTS FOR MAXIMIZING EXPRESSION | 0 | 0 |
| 1798 | 0 | 0 | 100 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A139-A139 KNOLL JH; CHUDLEY AE; GERRARD JW FREQUENCY AND REPLICATION PATTERN OF FRAGILE (X) (Q28) IN HETEROZYGOTES | 0 | 0 |
| 1799 | 0 | 2 | 101 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A144-A144 MIXON C; DEV VG INHIBITION OF FRAGILE-X EXPRESSION BY 5-AZACYTIDINE (AZA) AND BY S-ADENOSYLHOMOCYSTEINE (SAH) | 0 | 0 |
| 1800 | 0 | 0 | 104 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A161-A161 WILLEY A; HATCHER N; HEALY N FRAGILE-X FAMILIES - GENETIC INSTABILITY, OR UNEXPECTED CYTOGENETIC ABERRATIONS | 0 | 0 |