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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 17: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1601 | 6 | 15 | 1586 1997 GENETIC COUNSELING 8(1):1-6 Patsalis PC; Sismani C; Hadjimarcou MI; Rose N; Stylianidou G; Koukoulli R; Anastasiadou V; Deltas CC; Middleton L Cytogenetic and fragile X molecular testing of individuals with mental retardation of unknown etiology | 1 | 3 |
| 1602 | 18 | 37 | 1744 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):184-190 Patsalis PC; Sismani C; Hettinger JA; Boumba I; Georgiou I; Stylianidou G; Anastasiadou V; Koukoulli R; Pagoulatos G; Syrrou M Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: Incidence, genetic variation, and stability | 7 | 18 |
| 1603 | 2 | 3 | 2176 2002 NATURE REVIEWS GENETICS 3(1):4-5 Patterson M Twin-track approach to fragile X | 0 | 0 |
| 1604 | 8 | 31 | 498 1988 AMERICAN JOURNAL OF HUMAN GENETICS 43(5):684-688 PATTERSON M; BELL M; KRESS W; DAVIES KE; FROSTERISKENIUS U LINKAGE STUDIES IN A LARGE FRAGILE X-FAMILY | 10 | 23 |
| 1605 | 0 | 0 | 639 1989 GENOMICS 4(4):570-578 PATTERSON MN; BELL MV; BLOOMFIELD J; FLINT T; DORKINS H; THIBODEAU SN; SCHAID D; BREN G; SCHWARTZ CE; WIERINGA B; ROPERS HH; CALLEN DF; SUTHERLAND G; FROSTERISKENIUS U; VISSING H; DAVIES KE GENETIC AND PHYSICAL MAPPING OF A NOVEL REGION CLOSE TO THE FRAGILE X-SITE ON THE HUMAN X-CHROMOSOME | 17 | 43 |
| 1606 | 3 | 44 | 220 1984 JOURNAL OF SPEECH AND HEARING DISORDERS 49(3):328-332 PAUL R; COHEN DJ; BREG WR; WATSON M; HERMAN S FRAGILE-X SYNDROME - ITS RELATIONS TO SPEECH AND LANGUAGE DISORDERS | 12 | 16 |
| 1607 | 11 | 41 | 467 1987 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 17(4):457-468 PAUL R; DYKENS E; LECKMAN JF; WATSON M; BREG WR; COHEN DJ A COMPARISON OF LANGUAGE CHARACTERISTICS OF MENTALLY-RETARDED ADULTS WITH FRAGILE-X SYNDROME AND THOSE WITH NONSPECIFIC MENTAL-RETARDATION AND AUTISM | 19 | 26 |
| 1608 | 0 | 0 | 2282 2003 JOURNAL OF MEDICAL GENETICS 40:S80-S80 Payne S; Powell CM Fragile-X intermediate alleles - instability and inconclusion | 0 | 0 |
| 1609 | 0 | 0 | 360 1986 ANNALS OF NEUROLOGY 20(3):417-417 PAYTON JB; STEELE MW; WENGER SL; MINSHEW NJ ASSOCIATION OF THE FRAGILE-X CHROMOSOME ABNORMALITY WITH INFANTILE-AUTISM | 4 | 4 |
| 1610 | 10 | 16 | 649 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(3):417-421 PAYTON JB; STEELE MW; WENGER SL; MINSHEW NJ THE FRAGILE-X MARKER AND AUTISM IN PERSPECTIVE | 19 | 37 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1611 | 3 | 4 | 653 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(6):966-966 PAYTON JB; STEELE MW; WENGER SL; MINSHEW NJ FRAGILE-X AND AUTISM | 2 | 2 |
| 1612 | 11 | 81 | 1459 1996 BIOCHEMISTRY 35(15):5041-5053 Pearson CE; Sinden RR Alternative structures in duplex DNA formed within the trinucleotide repeats of the myotonic dystrophy and fragile X loci | 3 | 84 |
| 1613 | 23 | 30 | 1656 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 | 1 | 1 |
| 1614 | 0 | 0 | 1652 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:107-107 Peixoto A; Santos R; Seruca R; Amorim A; Castedo S Haplotype analysis in fragile X and normal Portuguese populations | 0 | 0 |
| 1615 | 10 | 14 | 1748 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):214-216 Pekarik V; Blazkova M; Kozak L Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic | 1 | 3 |
| 1616 | 0 | 0 | 1013 1992 PEDIATRIE 47(11):743-750 PELLISSIER MC; VOELCKEL MA; MATTEI JF FRAGILE-X SYNDROME - CURRENT KNOWLEDGE | 0 | 0 |
| 1617 | 12 | 18 | 799 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):367-369 PELLISSIER MC; VOELCKEL MA; PIQUET C; MATTEI MG; MATTEI JF TRANSMISSION OF MENTAL-RETARDATION WITH FRAGILE-X SITE BY 2 NORMAL TRANSMITTER BROTHERS | 0 | 0 |
| 1618 | 3 | 5 | 288 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 |
| 1619 | 0 | 0 | 217 1984 JOURNAL OF MEDICAL GENETICS 21(4):299-299 PEMBREY ME; WINTER RM; DAVIES KE A PERMUTATION THAT GENERATES THE DEFINITIVE MUTATION BY RECOMBINATION EXPLAINS THE INHERITANCE OF THE MARTIN-BELL SYNDROME (FRAGILE-X) | 9 | 13 |
| 1620 | 12 | 32 | 246 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 21(4):709-717 PEMBREY ME; WINTER RM; DAVIES KE A PRE-MUTATION THAT GENERATES A DEFECT AT CROSSING OVER EXPLAINS THE INHERITANCE OF FRAGILE X MENTAL RETARDATION | 82 | 116 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1621 | 24 | 48 | 410 1986 TRENDS IN NEUROSCIENCES 9(2):58-62 PEMBREY ME; WINTER RM; DAVIES KE FRAGILE X MENTAL-RETARDATION - CURRENT CONTROVERSIES | 7 | 9 |
| 1622 | 3 | 8 | 1787 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 |
| 1623 | 28 | 38 | 2317 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 128A(3):250-255 Penagarikano O; Gil A; Telez M; Ortega B; Flores P; Veiga I; Peixoto A; Criado B; Arrieta I A new insight into fragile X syndrome among Basque population | 0 | 0 |
| 1624 | 4 | 15 | 803 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):380-383 PERGOLIZZI R; BROWN WT; GOONEWARDENA P; BHAN R; DOBKIN C; DAHL N; PETTERSSON U MOLECULAR CHARACTERIZATION OF A DNA PROBE, U6.2, LOCATED CLOSE TO THE FRAGILE-X LOCUS | 0 | 0 |
| 1625 | 8 | 10 | 998 1992 LANCET 339(8788):271-272 PERGOLIZZI RG; ERSTER SH; GOONEWARDENA P; BROWN WT DETECTION OF FULL FRAGILE-X MUTATION | 46 | 69 |
| 1626 | 11 | 12 | 1408 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):176-180 Perroni L; Grasso M; Argusti A; LoNigro C; Croci GF; Zelante L; Garani GP; Bricarelli FD Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: A study of 87 families | 5 | 6 |
| 1627 | 1 | 1 | 1449 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 66(1):118-118 Perroni L; Grasso M; Argusti A; Nigro CL; Croci GF; Zelante L; Garani GP; Bricarelli FD Molecular and cytogenetic analysis of the fragile X syndrome in a series of 453 mentally retarded subjects: A study of 87 families (vol 64, pg 176, 1996) | 0 | 0 |
| 1628 | 0 | 0 | 1534 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A109-A109 Perroni L; Grasso M; Garavelli L; Argusti A; Cavani S; Lo Nigro C; Bricarelli FD Three cases of high functioning fragile X males | 0 | 0 |
| 1629 | 10 | 16 | 1592 1997 HUMAN GENETICS 101(2):186-189 Pesso R; Barkai G; Ravia Y; Gak E; Frydman M; Goldman B; Friedman E No founder effect detected in Jewish Ashkenazi patients with fragile-X syndrome | 2 | 3 |
| 1630 | 10 | 17 | 1961 2000 PRENATAL DIAGNOSIS 20(8):611-614 Pesso R; Berkenstadt H; Cuckle H; Gak E; Peleg L; Frydman M; Barkai G Screening for fragile X syndrome in women of reproductive age | 13 | 17 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1631 | 17 | 22 | 1751 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 |
| 1632 | 0 | 0 | 1927 2000 JOURNAL OF INVESTIGATIVE MEDICINE 48(1):11A-11A Peterson TL; Hagerman RJ; Tassone F Genotype-phenotype relationships in fragile X families. | 0 | 0 |
| 1633 | 0 | 18 | 510 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):77-82 PHELAN MC; STEVENSON RE; COLLINS JL; TRENT HE FRAGILE-X SYNDROME AND NEOPLASIA | 7 | 13 |
| 1634 | 17 | 51 | 2318 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 | 0 |
| 1635 | 10 | 15 | 840 1991 CELL 66(4):817-822 PIERETTI M; ZHANG FP; FU YH; WARREN ST; OOSTRA BA; CASKEY CT; NELSON DL ABSENCE OF EXPRESSION OF THE FMR-1 GENE IN FRAGILE-X SYNDROME | 291 | 583 |
| 1636 | 0 | 0 | 2135 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-232 Pietrobono R; Pomponi MG; Tabolacci E; Oostra B; Chiurazzi P; Neri G Quantitative analysis of DNA demethylation and trascriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine | 0 | 0 |
| 1637 | 16 | 36 | 2187 2002 NUCLEIC ACIDS RESEARCH 30(14):3278-3285 Pietrobono R; Pomponi MG; Tabolacci E; Oostra B; Chiurazzi P; Neri G Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine | 3 | 6 |
| 1638 | 59 | 96 | 1796 1999 INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE 3(6):639-645 Pimentel MMG Fragile X syndrome | 0 | 5 |
| 1639 | 8 | 12 | 1374 1995 JOURNAL OF MEDICAL GENETICS 32(11):907-908 PINTADO E; DEDIEGO Y; HMADCHA A; CARRASCO M; SIERRA J; LUCAS M INSTABILITY OF THE CGG REPEAT AT THE FRAXA LOCUS AND VARIABLE PHENOTYPIC-EXPRESSION IN A LARGE FRAGILE-X PEDIGREE | 2 | 9 |
| 1640 | 1 | 12 | 698 1990 CYTOMETRY 11(1):73-79 PIPER J; FANTES J; GOSDEN J; JI L AUTOMATIC DETECTION OF FRAGILE X-CHROMOSOMES USING AN X-CENTROMERE PROBE | 0 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1641 | 1 | 40 | 688 1990 ARCHIVES FRANCAISES DE PEDIATRIE 47(10):701-703 PIUSSAN C X-LINKED MENTAL-RETARDATION WITHOUT FRAGILE X-CHROMOSOME | 0 | 0 |
| 1642 | 3 | 18 | 1443 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):395-398 Piussan C; Mathieu M; Berquin P; Fryns JP Fragile X mutation and FG syndrome-like phenotype | 1 | 4 |
| 1643 | 24 | 53 | 876 1991 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 30(5):825-830 PIVEN J; GAYLE J; LANDA R; WZOREK M; FOLSTEIN S THE PREVALENCE OF FRAGILE-X IN A SAMPLE OF AUTISTIC INDIVIDUALS DIAGNOSED USING A STANDARDIZED INTERVIEW | 7 | 26 |
| 1644 | 4 | 15 | 1175 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):447-450 POMPONI MG; NERI G BUTYRATE AND ACETYL-CARNITINE INHIBIT THE CYTOGENETIC EXPRESSION OF THE FRAGILE-X IN-VITRO | 1 | 6 |
| 1645 | 8 | 9 | 1522 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):221-223 Ponsot G Fragile X syndrome. Early recognition. | 0 | 0 |
| 1646 | 1 | 6 | 80 1982 NEW ENGLAND JOURNAL OF MEDICINE 306(25):1551-1552 POPOVICH B; VEKEMANS M; ROSENBLATT D; MONROE P FRAGILE-X | 17 | 21 |
| 1647 | 5 | 26 | 87 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(5):869-878 POPOVICH BW; ROSENBLATT DS; COOPER BA; VEKEMANS M INTRACELLULAR FOLATE DISTRIBUTION IN CULTURED FIBROBLASTS FROM PATIENTS WITH THE FRAGILE-X SYNDROME | 8 | 12 |
| 1648 | 19 | 25 | 996 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 |
| 1649 | 25 | 37 | 959 1992 ANNALS OF MEDICINE 24(6):453-456 POUSTKA A FRAGILE-X SYNDROME - MOLECULAR ANALYSIS REVEALS A NEW MECHANISM OF MUTATION IN HUMAN GENETIC-DISEASES | 0 | 0 |
| 1650 | 0 | 4 | 855 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2082-2082 POUSTKA A; DIETRICH A; KIOSCHIS P; KORN B; GROSS B; MONACO A; TONIOLO D; WARREN S; LEHRACH H MOLECULAR CHARACTERIZATION OF THE FRAGILE-X REGION | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1651 | 0 | 0 | 742 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):75-75 POUSTKA A; DIETRICH A; KORN B; GROSS B; MONACO A; TONIOLO D; WARREN S; LEHRACH H MOLECULAR CHARACTERIZATION OF THE FRAGILE-X REGION | 0 | 0 |
| 1652 | 12 | 37 | 894 1991 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 88(19):8302-8306 POUSTKA A; DIETRICH A; LANGENSTEIN G; TONIOLO D; WARREN ST; LEHRACH H PHYSICAL MAP OF HUMAN XQ27-QTER - LOCALIZING THE REGION OF THE FRAGILE-X MUTATION | 7 | 75 |
| 1653 | 5 | 12 | 1614 1997 JOURNAL OF SPECIAL EDUCATION 31(3):362-376 Powell L; Houghton S; Douglas G Comparison of etiology-specific cognitive functioning profiles for individuals with fragile X and individuals with Down syndrome | 2 | 4 |
| 1654 | 8 | 19 | 1003 1992 MEDICINA CLINICA 98(4):131-133 PRIETO F; MARTINEZCASTELLANO F THE FRAGILE-X SYNDROME AND ITS RELATION WITH OTHER SYNDROMES LINKED TO CHROMOSOME-X ASSOCIATED WITH MENTAL-RETARDATION | 0 | 0 |
| 1655 | 27 | 41 | 2196 2002 RNA-A PUBLICATION OF THE RNA SOCIETY 8(12):1482-1488 Primerano B; Tassone F; Hagerman RJ; Hagerman P; Amaldi F; Bagni C Reduced FMR1 mRNA translation efficiency in Fragile X patients with premutations | 6 | 10 |
| 1656 | 3 | 11 | 368 1986 BRITISH JOURNAL OF PSYCHIATRY 148:655-657 PRIMROSE DA; ELMATMATI R; BOYD E; GOSDEN C; NEWTON M PREVALENCE OF THE FRAGILE-X SYNDROME IN AN INSTITUTION FOR THE MENTALLY-HANDICAPPED | 16 | 22 |
| 1657 | 11 | 13 | 1294 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 55(3):384-386 PRIOR TW; PAPP AC; SNYDER PJ; SEDRA MS; GUIDA M; ENRILE BG GERMLINE MOSAICISM AT THE FRAGILE-X LOCUS | 2 | 7 |
| 1658 | 0 | 23 | 21 1981 JOURNAL OF MEDICAL GENETICS 18(5):366-373 PROOPS R; WEBB T THE FRAGILE X-CHROMOSOME IN THE MARTIN-BELL-RENPENNING SYNDROME AND IN MALES WITH OTHER FORMS OF FAMILIAL MENTAL-RETARDATION | 20 | 32 |
| 1659 | 16 | 49 | 515 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):123-142 PROUTY LA; ROGERS RC; STEVENSON RE; DEAN JH; PALMER KK; SIMENSEN RJ; COSTON GN; SCHWARTZ CE FRAGILE-X SYNDROME - GROWTH, DEVELOPMENT, AND INTELLECTUAL FUNCTION | 28 | 36 |
| 1660 | 0 | 0 | 277 1985 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 27(1):95-96 PUESCHEL SM; FINELLI PV NEUROLOGICAL INVESTIGATIONS IN PATIENTS WITH FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1661 | 0 | 0 | 33 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 |
| 1662 | 0 | 36 | 110 1983 AMERICAN JOURNAL OF MENTAL DEFICIENCY 87(4):372-376 PUESCHEL SM; HAYS RM; MENDOZA T FAMILIAL X-LINKED MENTAL-RETARDATION SYNDROME ASSOCIATED WITH MINOR CONGENITAL-ANOMALIES, MACRO-ORCHIDISM, AND FRAGILE X-CHROMOSOME | 6 | 8 |
| 1663 | 5 | 17 | 292 1985 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 15(3):335-338 PUESCHEL SM; HERMAN R; GRODEN G SCREENING-CHILDREN WITH AUTISM FOR FRAGILE-X SYNDROME AND PHENYLKETONURIA | 15 | 25 |
| 1664 | 4 | 18 | 476 1987 JOURNAL OF MENTAL DEFICIENCY RESEARCH 31:73-79 PUESCHEL SM; OBRIEN MM; PADREMENDOZA T KLINEFELTER SYNDROME AND ASSOCIATED FRAGILE-X SYNDROME | 7 | 8 |
| 1665 | 14 | 17 | 1194 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):370-373 PUISSANT H; MALINGE MC; LARGETPIET A; MARTIN D; CHAUVEAU P; ODENT S; PLESSIS G; PARENT P; LEMAREC B; LARGETPIET L MOLECULAR ANALYSIS OF 53 FRAGILE-X FAMILIES WITH THE PROBE-STB12.3 | 1 | 2 |
| 1666 | 0 | 0 | 1279 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1300-1300 PULKKINEN L; MANNERMAA A; KAJANOJA E; RYYNANANEN M; SAARIKOSKI S DELETION IN THE FMR1 GENE IN A FRAGILE-X-MALE | 0 | 0 |
| 1667 | 0 | 0 | 2359 2004 MOVEMENT DISORDERS 19:S444-S444 Puong K; Zhao Y; Law H; Wong M; Ng I; Tan E Screening for Fragile X premutation alleles in patients with essential tremor | 0 | 0 |
| 1668 | 0 | 4 | 275 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):726-726 PURRELLO M; ALHADEFF B; ROCCHI M; ARCHIDIACONO N; DRAYNA D; SINISCALCO M RELATIVE POSITIVE OF POLYMORPHIC DNA LOCI OF THE HUMAN X-CHROMOSOME LONG ARM SUBTELOMERIC REGION WITH RESPECT TO THE FRAGILE X SITE (FRAXQ27) | 1 | 4 |
| 1669 | 0 | 0 | 564 1988 AUSTRALIAN PAEDIATRIC JOURNAL 24(1):96-96 PURVISSMITH S; LAING S; STEWART L; TURNER G; WASS D; SUTHERLAND G; LEVERSHA M PRENATAL-DIAGNOSIS OF FRAGILE-X | 0 | 0 |
| 1670 | 11 | 14 | 525 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):337-345 PURVISSMITH SG; LAING S; SUTHERLAND GR; BAKER E PRENATAL-DIAGNOSIS OF THE FRAGILE-X - THE AUSTRALASIAN EXPERIENCE | 0 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1671 | 8 | 46 | 67 1982 JOHNS HOPKINS MEDICAL JOURNAL 151(5):231-237 PYERITZ RE; STAMBERG J; THOMAS GH; BELL BB; ZAHKA KG; BERNHARDT BA THE MARKER XQ28 SYNDROME (FRAGILE-X SYNDROME) IN A RETARDED MAN WITH MITRAL-VALVE PROLAPSE | 8 | 13 |
| 1672 | 23 | 52 | 2194 2002 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 99(24):15758-15763 Qin M; Kang J; Smith CB Increased rates of cerebral glucose metabolism in a mouse model of fragile X mental retardation | 3 | 4 |
| 1673 | 0 | 0 | 2263 2003 DEVELOPMENTAL BIOLOGY 259(2):528-529 Qin M; Kang J; Smith CB Increased local rates of cerebral protein synthesis in fragile X knockout mice. | 0 | 0 |
| 1674 | 18 | 31 | 1358 1995 HUMAN MOLECULAR GENETICS 4(9):1681-1684 QUAN F; GROMPE M; JAKOBS P; POPOVICH BW SPONTANEOUS DELETION IN THE FMR1 GENE IN A PATIENT WITH FRAGILE-X SYNDROME AND CHERUBISM | 7 | 13 |
| 1675 | 20 | 37 | 1259 1995 AMERICAN JOURNAL OF HUMAN GENETICS 56(5):1042-1051 QUAN F; ZONANA J; GUNTER K; PETERSON KL; MAGENIS RE; POPOVICH BW AN ATYPICAL CASE OF FRAGILE-X SYNDROME CAUSED BY A DELETION THAT INCLUDES THE FMRI GENE | 16 | 29 |
| 1676 | 0 | 0 | 1319 1995 CLINICAL CHEMISTRY 41(11):30-30 RADU DN; CHIANG CS RAPID, NONRADIOACTIVE SOUTHERN BLOT METHOD FOR DETECTING FRAGILE-X MUTATIONS | 0 | 0 |
| 1677 | 0 | 0 | 1113 1993 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 37:201-202 RAEBURN S PIECING TOGETHER THE FRAGILE-X - FRAGILE-X WORKSHOP, ROYAL-SOCIETY-OF-MEDICINE, LONDON, ENGLAND, 1 JULY 1992 | 0 | 0 |
| 1678 | 0 | 0 | 763 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):287-287 RAFI SK; SURANA RB; ANDERSON LH; CHRISTOPHER KL; WILSON B; MEHM WJ HYPEROXIA ENHANCES THE INDUCTION OF FRAGILE-X SITE OF THE FRAGILE-X SYNDROME | 0 | 0 |
| 1679 | 10 | 27 | 699 1990 EUROPEAN NEUROLOGY 30(1):32-37 RAIMONDI E; LENTI C; ROMAGNONI M; NEGRI R; GAMBINI E; MUSETTI L; DECARLI L FRAGILE-X MENTAL-RETARDATION IN A LARGE 5-GENERATION FAMILY - A CLINICAL AND CYTOGENETIC STUDY | 0 | 0 |
| 1680 | 8 | 19 | 905 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1681 | 23 | 29 | 1023 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(11):1231-1235 RAMOS FJ; EUNPU DL; FINUCANE B; PFENDNER EG DIRECT DNA TESTING FOR FRAGILE-X SYNDROME | 1 | 2 |
| 1682 | 0 | 0 | 1846 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):360-360 Ramos FJ; Mila M; Ortilles M; Rife M; Tazon B; De Diego Y; Willemsen R Validity of the analysis of the FMRP expression in bloodsmears as a screening method for the Fragile X Syndrome. | 1 | 1 |
| 1683 | 11 | 15 | 2241 2003 ARCHIVES DE PEDIATRIE 10(5):401-402 Ramos FJ; Willemsen R Diagnosis of the Fragile X Syndrome by the analysis of FMRP expression in blood and hair roots | 0 | 0 |
| 1684 | 19 | 22 | 2058 2001 REVISTA DE NEUROLOGIA 33:S9-S13 Ramos-Fuentes FJ New methods for the diagnosis of fragile X syndrome: A study of the FMRP in blood and hair | 0 | 0 |
| 1685 | 0 | 0 | 748 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):158-158 RAMZY MI; SALINAS CF ORODENTAL FINDINGS IN AN EGYPTIAN SAMPLE OF FRAGILE-X CASES | 0 | 0 |
| 1686 | 0 | 0 | 1271 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):692-692 RANCHINO B; TARAVATH A; KALICHMAN M; BURTON BB; MCCORQUODALE MM; MCCORQUODALE DJ SELECTION AGAINST A MARKER CHROMOSOME IN FRAGILE-X-STRESSED CULTURES | 0 | 0 |
| 1687 | 2 | 3 | 2146 2002 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 32(1):60-61 Rapin I Legitimacy of comparing fragile X with autism questioned | 0 | 0 |
| 1688 | 2 | 23 | 1337 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):345-352 Rattazzi MC Protein therapy in fragile X syndrome - A brief overview of principles, potentials and problems | 0 | 0 |
| 1689 | 7 | 66 | 2352 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):75-81 Rattazzi MC; LaFauci G; Brown WT Prospects for gene therapy in the fragile X syndrome | 0 | 0 |
| 1690 | 0 | 0 | 1052 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1502-1502 RAVIA Y; PESSO R; BRAIERGOLDSTEIN O; BRAND N; BARKAI G; GOLDMAN B SCREENING FOR FRAGILE-X MUTATION IN MENTALLY-RETARDED INDIVIDUALS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1691 | 0 | 0 | 2212 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):372-372 Reddy K Autism: Incidence of cytogenetic abnormality and fragile-X syndrome. | 0 | 0 |
| 1692 | 2 | 4 | 689 1990 ARCHIVES OF DISEASE IN CHILDHOOD 65(3):335-335 REDINGTON A; BUSH A FRAGILE-X MENTAL-RETARDATION | 2 | 2 |
| 1693 | 3 | 12 | 1142 1993 NEUROPEDIATRICS 24(4):211-213 REES M; DIEBOLD U; PARKER K; DOOSE H; GARDINER RM; WHITEHOUSE WP BENIGN CHILDHOOD EPILEPSY WITH CENTROTEMPORAL SPIKES AND THE FOCAL SHARP WAVE TRAIT IS NOT LINKED TO THE FRAGILE-X REGION | 6 | 23 |
| 1694 | 2 | 10 | 204 1984 HUMAN GENETICS 68(2):189-190 REIDY JA; CHEN ATL FOLIC-ACID AND CHROMOSOME BREAKAGE .2. A METHIONINE EFFECT SIMILAR TO THAT IN FRAGILE-X EXPRESSION | 1 | 9 |
| 1695 | 0 | 0 | 777 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):417-417 REINER O; VERKERK AJMH; PIERETTI M; PIZZUTI A; BLONDE L; NELSON D; OOSTRA B; CASKEY CT CHARACTERIZATION OF EXPRESSED SEQUENCES AT THE FRAGILE-X LOCUS | 0 | 0 |
| 1696 | 0 | 0 | 749 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):159-159 REISS A; FREUND L; AYLWARD E NEUROANATOMY OF THE FRAGILE X SYNDROME | 0 | 0 |
| 1697 | 0 | 0 | 1310 1995 BIOLOGICAL PSYCHIATRY 37(9):629-629 REISS AL FRAGILE-X SYNDROME | 0 | 0 |
| 1698 | 4 | 31 | 833 1991 ANNALS OF NEUROLOGY 29(1):26-32 REISS AL; AYLWARD E; FREUND LS; JOSHI PK; BRYAN RN NEUROANATOMY OF FRAGILE-X-SYNDROME - THE POSTERIOR-FOSSA | 54 | 110 |
| 1699 | 2 | 9 | 911 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):61-64 REISS AL; CIANCHETTI C; COHEN IL; DEVRIES B; HAGERMAN R; HINTON V; FROSTER U; LACHIEWICZ A; MAZZOCCO M; SOBESKY W; SUDHALTER V BRIEF SCREENING QUESTIONNAIRE FOR DETERMINING AFFECTED STATE IN FRAGILE-X SYNDROME - A CONSENSUS RECOMMENDATION | 2 | 3 |
| 1700 | 150 | 233 | 2262 2003 DEVELOPMENT AND PSYCHOPATHOLOGY 15(4):927-968 Reiss AL; Dant CC The behavioral neurogenetics of fragile X syndrome: Analyzing gene-brain-behavior relationships in child developmental psychopathologies | 0 | 0 |
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