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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by year, source, volume, issue, page.
Page 16: 1 (1) 2 (101) 3 (201) 4 (301) 5 (401) 6 (501) 7 (601) 8 (701) 9 (801) 10 (901) 11 (1001) 12 (1101) 13 (1201) 14 (1301) 15 (1401) 16 (1501) 17 (1601) 18 (1701) 19 (1801) 20 (1901) 21 (2001) 22 (2101) 23 (2201) 24 (2301)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1501 | 4 | 138 | 1501 1996 MEDICAL HYPOTHESES 47(4):289-298 Fischer KM Genes for Prader Willi Syndrome Angelman syndrome and fragile X syndrome are homologous, with genetic imprinting and unstable trinucleotide repeats causing mental retardation, autism and aggression | 0 | 4 |
| 1502 | 16 | 57 | 1502 1996 MOLECULAR AND CELLULAR BIOLOGY 16(7):3825-3832 Siomi MC; Zhang Y; Siomi H; Dreyfuss G Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them | 48 | 98 |
| 1503 | 10 | 31 | 1503 1996 NATURE GENETICS 12(1):91-93 Khandjian EW; Corbin F; Woerly S; Rousseau F The fragile X mental retardation protein is associated with ribosomes | 58 | 93 |
| 1504 | 13 | 45 | 1504 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 |
| 1505 | 5 | 27 | 1505 1996 NUCLEIC ACIDS RESEARCH 24(4):784-792 Mariappan SVS; Catasti P; Chen X; Ratliff R; Moyzis RK; Bradbury EM; Gupta G Solution structures of the individual single strands of the fragile X DNA triplets (GCC)(n)center dot(GGC)(n) | 10 | 48 |
| 1506 | 12 | 14 | 1506 1996 PEDIATRIC NEUROLOGY 15(4):358-360 Kluger G; Bohm I; Laub MC; Waldenmaier C Epilepsy and fragile X gene mutations | 6 | 12 |
| 1507 | 0 | 0 | 1507 1996 PEDIATRIC RESEARCH 39(2):371-371 Torrado M; Herrera J; Chertkoff L; Tenembaum S; Bin L; Barreiro C Diagnosis value of a pediatric clinical score for the diagnosis of the Fragile X Syndrome | 0 | 0 |
| 1508 | 24 | 29 | 1508 1996 PEDIATRICS 97(1):122-126 Hagerman RJ; Staley LW; OConner R; Lugenbeel K; Nelson D; McLean SD; Taylor A Learning-disabled males with a fragile X CGG expansion in the upper premutation size range | 25 | 35 |
| 1509 | 14 | 17 | 1509 1996 PEDIATRICS 98(2):297-300 Desposito F; Cho S; Frias JL; Sherman J; Wappner RS; Wilson MG Health supervision for children with fragile X syndrome | 3 | 8 |
| 1510 | 35 | 63 | 1510 1996 PRENATAL DIAGNOSIS 16(13):1199-1211 Sutherland GR; Mulley JC Fragile X syndrome and Fragile XE mental retardation | 3 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1511 | 16 | 28 | 1511 1996 PSYCHIATRIC GENETICS 6(2):81-86 Ashworth A; Abusaad I; Walsh C; Nanko S; Murray RM; Asherson P; McGuffin P; Gill M; Owen MJ; Collier DA Linkage analysis of the fragile X gene FMR-1 and schizophrenia: No evidence for linkage but report of a family with schizophrenia and an unstable triplet repeat | 1 | 3 |
| 1512 | 8 | 27 | 1512 1996 PSYCHIATRY RESEARCH 64(2):97-104 Thompson NM; Rogeness GA; McClure E; Clayton R; Johnson C Influence of depression on cognitive functioning in Fragile X females | 1 | 5 |
| 1513 | 23 | 49 | 1513 1996 REVISTA MEDICA DE CHILE 124(7):865-872 Jara L; Avendano I; Aspillaga M; Blanco R Molecular and genetic features of fragile X syndrome. A review | 0 | 0 |
| 1514 | 27 | 77 | 1514 1996 SCREENING 4(4):175-192 Meadows KL; Sherman SL Fragile X syndrome: Examination of issues pertaining to population-based screening | 2 | 2 |
| 1515 | 17 | 35 | 1515 1996 SOMATIC CELL AND MOLECULAR GENETICS 22(6):435-441 Eberhart DE; Warren ST Nuclease sensitivity of permeabilized cells confirms altered chromatin formation at the fragile X locus | 6 | 14 |
| 1516 | 17 | 33 | 1516 1996 VARIATION IN THE HUMAN GENOME 197:119-126 Sutherland GR; Richards RI Unusual inheritance patterns due to dynamic mutation in fragile X syndrome | 0 | 0 |
| 1517 | 5 | 20 | 1517 1996 VARIATION IN THE HUMAN GENOME 197:126-136 Weiss KM; Sutherland GR; Harper PS; Bodmer W; Bowcock AM; Freimer NB; Kidd KK; Chakraborty R; Armour J; Donnelly P; Clark A; Chakravarti A; Weatherall DJ; Edwards JH; Balmain A; Zechner R Unusual inheritance patterns due to dynamic mutation in fragile X syndrome - Discussion | 0 | 0 |
| 1518 | 0 | 1 | 1518 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):191-192 Fombonne E The fragile X syndrome | 0 | 0 |
| 1519 | 13 | 25 | 1519 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):195-201 Mandel JL The fragile X mental retardation syndrome: the FMR1 gene and its mutations | 0 | 0 |
| 1520 | 13 | 24 | 1520 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):202-208 Hagerman RJ Fragile X syndrome: meeting the challenges of diagnosis and care | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1521 | 12 | 16 | 1521 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):209-212 Fombonne E Epidemiological studies of fragile X syndrome | 0 | 0 |
| 1522 | 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 |
| 1523 | 6 | 9 | 1523 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):224-226 Gerard CL; Guillotte E; Servel F; Barbeau M Assessment and remediation of communication disorders in children with fragile X syndrome | 0 | 0 |
| 1524 | 3 | 10 | 1524 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):227-231 Roge B Fragile X syndrome. Special education: the French context | 0 | 0 |
| 1525 | 13 | 27 | 1525 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):232-238 Turk J Treatments and services for individuals with fragile X syndrome and their families | 0 | 0 |
| 1526 | 24 | 41 | 1526 1997 AMERICAN JOURNAL OF HUMAN GENETICS 60(1):103-112 FalikZaccai TC; Shachak E; Yalon M; Lis Z; Borochowitz Z; Macpherson JN; Nelson DL; Eichler EE Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype | 15 | 26 |
| 1527 | 22 | 35 | 1527 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(3):660-667 deVries BBA; vandenOuweland AMW; Mohkamsing S; Duivenvoorden HJ; Mol E; Gelsema K; vanRijn M; Halley DJJ; Sandkuijl LA; Oostra BA; Tibben A; Niermeijer MF Screening and diagnosis for the fragile X syndrome among the mentally retarded: An epidemiological and psychological survey | 35 | 70 |
| 1528 | 0 | 0 | 1528 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A6-A6 Fisch GS; Holden JJA; Chalifoux M; Carpenter NJ; Howard-Peebles PN; Maddalena A; Simensen R; Tarleton J; Borghgraef M; Steyaert J; Fryns JP Natural history of cognitive and adaptive behavior in young fragile X males and females: A 6-year prospective multicenter study. | 0 | 0 |
| 1529 | 0 | 0 | 1529 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A6-A6 Kenneson A; Cramer DW; Warren ST The fragile X premutation is not a major risk for early menopause. | 0 | 0 |
| 1530 | 0 | 0 | 1530 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A26-A26 Corbin F; Bouillon M; Rousseau F; Khandjian EW The fragile-X mental retardation protein is a mRNA chaperone associated with translating complexes. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1531 | 0 | 0 | 1531 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A26-A26 Brown VL; Small K; Lakkis L; Wilkinson KD; Warren ST Purification and characterization of the fragile X mental retardation protein. | 0 | 0 |
| 1532 | 0 | 0 | 1532 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A33-A33 Ju W; Xu WM; Hwang YW; Brown WT; Zhong N Molecular pathogenetic studies of the fragile X syndrome: Double knockouts of FMR1 and FXR1 affect early development of Xenopus oocytes. | 0 | 0 |
| 1533 | 0 | 0 | 1533 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A100-A100 Hagerman RJ; Staley-Gane L; Linden MG; Tassone F; Hills J; Taylor AK A compound heterozygous female with fragile X syndrome. | 0 | 0 |
| 1534 | 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 |
| 1535 | 0 | 0 | 1535 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A110-A110 Rhee LE; Hatcher SL; Robb KM; Towner DR Fragile X syndrome associated with birth defects. | 0 | 0 |
| 1536 | 0 | 0 | 1536 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A128-A128 Jenkins EC; Wen GY; Goldberg EM; Genovese M; Brown WT; Wisniewski HM Fragile X chromosome longitudinal sections studied by transmission electron microscopy. | 0 | 0 |
| 1537 | 0 | 0 | 1537 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A160-A160 Osthus RC; DiMaio MS; Mahoney MJ; Bale AE Significance of borderline fragile X premutations. | 0 | 0 |
| 1538 | 0 | 0 | 1538 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A160-A160 Paradee W; Rasmussen D; Melikian H; Conn PJ; Warren ST Hippocampus-independent deficits in the Fragile X mouse. | 0 | 0 |
| 1539 | 0 | 0 | 1539 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A170-A170 Feng Y; Absher D; Brown V; Eberhart DE; Malter HE; Warren ST FMRP associates with polyribosomes as an mRNP and the I304N mutation causing severe fragile X syndrome abolishes this association. | 0 | 0 |
| 1540 | 0 | 0 | 1540 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A175-A175 Kaufmann WE; Abrams MT; Chen W; Reiss AL Genotype and molecular phenotype in fragile X syndrome. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1541 | 0 | 0 | 1541 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A192-A192 Staley-Gane L; Holloway SL; Flynn L; Logan L; Hageman RJ Assessment of patient agenda prior to genetic counseling for fragile X syndrome. | 0 | 0 |
| 1542 | 0 | 0 | 1542 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A219-A219 de Vries BBA; van den Ouweland AMW; Mohkamsing S; Duivenvoorden HJ; Halley DJJ; Sandkuijl LA; Oostra BA; Tibben A; Niermeijer MF A fragile X screening program in The Netherlands: prevalence of fragile X syndrome lower than previously considered, but the disorder is still underdiagnosed. | 0 | 0 |
| 1543 | 0 | 0 | 1543 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A304-A304 Bat O; Kimmel M; Axelrod DE; Chakraborty R Computer simulation of expansions of DNA triplet repeats in the fragile X syndrome and Huntington's disease. | 0 | 0 |
| 1544 | 0 | 0 | 1544 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 |
| 1545 | 0 | 0 | 1545 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A313-A313 Layman LC; Moffitt DV; McDonough PG; Song M; Shamoun D; Ledbetter DH; Das S Correlation and vertical transmission of fragile X syndrome and ovarian failure within a single family. | 0 | 0 |
| 1546 | 0 | 0 | 1546 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A321-A321 Tassone F; Hagerman RJ; Ikle D; Dyer PN; Lampe M; Willemsen R; Oostra BA; Taylor AK FMRP expression as a potential prognostic indicator in fragile X syndrome. | 1 | 1 |
| 1547 | 0 | 0 | 1547 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A324-A324 Zhong N; Ju W; Xu WM; Liu B; Dobkin C; Brown WT Molecular pathogenetic studies of the fragile X syndrome: A candidate transcript targeted by the fragile X protein FMRP. | 0 | 0 |
| 1548 | 0 | 0 | 1548 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A330-A330 Das S; Kubota T; Song M; Daniel R; Berry-Kravis EM; Popovich B; Prior TW; Arinami T; Ravine D; Ledbetter DH Methylation analysis of the fragile X syndrome by PCR. | 0 | 0 |
| 1549 | 0 | 0 | 1549 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A389-A389 Ye LL; Ju W; Xu WM; Schupf N; Jenkins EC; Brown WT; Zhong N Distribution of apolipoprotein E genotypes in the fragile X syndrome, Batten disease, and Down syndrome populations. | 0 | 0 |
| 1550 | 0 | 0 | 1550 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A407-A407 Sucharov CC; Varandas FR; Rondinelli E; Carakushansky G; Moura-Neto RS Establishment of a differential diagnostic of patients with Mental Retardation based on Southern-blot and PCR considering the frequency of Fragile X trinucleotide repeats from normal population in Rio de Janeiro, Brazil. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1551 | 0 | 0 | 1551 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A407-A407 Taylor AK; Tassone F; Staley-Gane L; Hagerman RJ Identical premutation size in multiple tissues of a male fragile X carrier. | 0 | 0 |
| 1552 | 30 | 43 | 1552 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(6):1362-1369 Kenneson A; Cramer DW; Warren ST Fragile X premutations are not a major cause of early menopause | 11 | 22 |
| 1553 | 8 | 29 | 1553 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 68(1):62-69 McConkieRosell A; Spiridigliozzi GA; Iafolla T; Tarleton J; Lachiewicz AM Carrier testing in the fragile X syndrome: Attitudes and opinions of obligate carriers | 7 | 13 |
| 1554 | 3 | 14 | 1554 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 68(4):445-449 Wen GY; Jenkins EC; Yao XL; Yoon D; Brown WT; Wisniewski HM Transmission electron microscopy of chromosomes by longitudinal section preparation: Application to fragile X chromosome analysis | 3 | 5 |
| 1555 | 3 | 11 | 1555 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 69(1):114-116 Martin NG; Healey SC; Pangan TS; Heath AC; Turner G Do mothers of dizygotic twins have earlier menopause? A role for fragile X? | 5 | 12 |
| 1556 | 8 | 13 | 1556 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 72(2):245-246 Healey SC; Duffy DL; Martin NG; Turner G Is fragile X syndrome a risk factor for dizygotic twinning? | 2 | 4 |
| 1557 | 21 | 25 | 1557 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 72(4):430-434 Hammond LS; Macias MM; Tarleton JC; Pai GS Fragile X syndrome and deletions in FMR1: New case and review of the literature | 13 | 21 |
| 1558 | 12 | 39 | 1558 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 74(2):167-171 Miezejeski CM; Heaney G; Belser R; Brown WT; Jenkins EC; Sersen EA Longer brainstem auditory evoked response latencies of individuals with fragile X syndrome related to sedation | 0 | 0 |
| 1559 | 0 | 0 | 1559 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 74(6):568-568 Bleiweiss H; Pollini A; Goldemberg A; Schuarzberg C; Staszauer M; Bleiweiss D Treatment of patients with fragile X syndrome and psychiatric abnormalities. | 0 | 0 |
| 1560 | 0 | 0 | 1560 1997 AMERICAN JOURNAL OF PATHOLOGY 151(5):G3-G3 Shrimpton AE; Hicks K; Lamberson CM Fragile X syndrome molecular detection. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1561 | 22 | 32 | 1561 1997 ANNALES DE GENETIQUE 40(3):139-144 Gerard B; LeHeuzey MF; Brunie G; Lewine P; Saiag MC; Cacheux V; DaSilva F; Dugas M; MourenSimeoni MC; Elion J; Grandchamp B Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded children | 3 | 7 |
| 1562 | 2 | 15 | 1562 1997 ANNALES MEDICO-PSYCHOLOGIQUES 155(7):457-460 BillonGalland IO The fragile X syndrome and its clinical psychotic expression | 0 | 0 |
| 1563 | 0 | 0 | 1563 1997 ANNALES MEDICO-PSYCHOLOGIQUES 155(7):460-460 Koupernik; Doutheau; Rapporteur The fragile X syndrome and its clinical psychotic expression - Discussion | 0 | 0 |
| 1564 | 6 | 10 | 1564 1997 ANNALS OF CLINICAL BIOCHEMISTRY 34:517-520 Chen TA; Lu XF; Che PK; Ho WKK Variation of the CGG repeat in FMR-1 gene in normal and fragile X Chinese subjects | 5 | 7 |
| 1565 | 24 | 43 | 1565 1997 ANNALS OF MEDICINE 29(6):563-567 Oostra BA; Hoogeveen AT Animal model for fragile X syndrome | 2 | 8 |
| 1566 | 0 | 0 | 1566 1997 ARCHIVES DE PEDIATRIE 4(2):195-195 Mornet E Fragile X syndrome - Response | 0 | 0 |
| 1567 | 1 | 1 | 1567 1997 ARCHIVES DE PEDIATRIE 4(2):195-195 Beauvais P Fragile X syndrome | 0 | 0 |
| 1568 | 17 | 20 | 1568 1997 ARCHIVES DE PEDIATRIE 4(3):227-236 Cossee M; Moutou C; Biancalana V; Bouix JC; Plessis G; Delobel B; Croquette MF; Gilgenkrantz S; Lambert JC; Malpuech G; Stoll C; Lanoe JL; Pechevis M; Mandel JL The fragile X syndrome is still underdiagnosed: Efficacy of molecular testing in mentally retarded probands | 2 | 2 |
| 1569 | 2 | 23 | 1569 1997 ARCHIVES OF DISEASE IN CHILDHOOD 76(3):264-267 Corrigan N; Stewart M; Scott M; Fee F Fragile X, iron, and neurodevelopmental screening in 8 year old children with mild to moderate learning difficulties | 0 | 4 |
| 1570 | 1 | 1 | 1570 1997 ARCHIVES OF MEDICAL RESEARCH 28(1):149-149 Rivera H Fragile X studies and authorship (vol 27, pg 587, 1996) | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1571 | 25 | 35 | 1571 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 |
| 1572 | 0 | 0 | 1572 1997 BRITISH MEDICAL JOURNAL 315(7102):208-208 White C Screening for fragile X is cost effective and accurate | 0 | 0 |
| 1573 | 4 | 11 | 1573 1997 BRITISH MEDICAL JOURNAL 315(7117):1174-1175 Barnicoat A Screening for fragile X syndrome: a model for genetic disorders? | 1 | 4 |
| 1574 | 8 | 10 | 1574 1997 BRITISH MEDICAL JOURNAL 315(7117):1223-1226 Turner G; Robinson H; Wake S; Laing S; Partington M Case finding for the fragile X syndrome and its consequences | 5 | 9 |
| 1575 | 18 | 26 | 1575 1997 CLINICAL GENETICS 51(1):1-6 Loesch DZ; Petrovic V; Francis DI; Oertel R; Slater H ''Reduction'' of CGG trinucleotide expansion from mother to offspring in seven fragile-X families | 4 | 7 |
| 1576 | 1 | 9 | 1576 1997 CLINICAL GENETICS 51(1):71-74 Behjati F; Mullarkey M; Bergbaum A; Berry AC; Docherty Z Chromosome deletion 17p11.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigation | 0 | 5 |
| 1577 | 9 | 15 | 1577 1997 CLINICAL GENETICS 52(3):147-154 Hecimovic S; Barisic I; Muller A; Petkovic I; Baric I; Ligutic I; Pavelic K Expand long PCR for fragile X mutation detection | 8 | 23 |
| 1578 | 11 | 14 | 1578 1997 CLINICAL GENETICS 52(4):211-215 Arvio M; Peippo M; Simola KOJ Applicability of a checklist for clinical screening of the fragile X syndrome | 10 | 13 |
| 1579 | 39 | 64 | 1579 1997 CURRENT OPINION IN NEUROLOGY 10(2):142-147 Chakrabarti L; Davies KE Fragile X syndrome | 2 | 4 |
| 1580 | 0 | 0 | 1580 1997 CYTOGENETICS AND CELL GENETICS 77(1-2):P250-P250 Malarchuk S; Li S; Wertelecki W; Bychkova A; Livshits L Analysis of patients with fragile X syndrome in Ukraine. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1581 | 0 | 0 | 1581 1997 CYTOGENETICS AND CELL GENETICS 77(1-2):P287-P287 Tengstrom C; Ikonen A; Kaski M; Autio S High resolution banding and fragile X - screening in persons with mild mental retardation. | 0 | 0 |
| 1582 | 10 | 16 | 1582 1997 DIAGNOSTIC MOLECULAR PATHOLOGY 6(3):161-166 Marini T; Pflueger S; Jackson A; Naber S; Karpells S; Naeem R A five-year experience with fragile X testing - Setting laboratory standards of practice and a cost-effective protocol | 1 | 2 |
| 1583 | 1 | 1 | 1583 1997 DIAGNOSTIC MOLECULAR PATHOLOGY 6(5):304-304 Marini T; Pflueger S; Jackson A; Naber S; Karpells S; Naeem R Five-year experience with Fragile X-testing - Setting laboratory standards of practice and a cost-effective protocol (vol 6, pg 161, 1997) | 0 | 0 |
| 1584 | 10 | 28 | 1584 1997 EUROPEAN JOURNAL OF HUMAN GENETICS 5(2):89-93 FulchignoniLataud MC; Olchwang S; Serre JL The fragile X CGG repeat shows a marked level of instability in hereditary non-polyposis colorectal cancer patients | 1 | 6 |
| 1585 | 26 | 48 | 1585 1997 FOLIA HISTOCHEMICA ET CYTOBIOLOGICA 35(3):135-141 Szot M The fragile X syndrome | 0 | 0 |
| 1586 | 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 |
| 1587 | 11 | 19 | 1587 1997 GENETIC TESTING 1(3):151-155 Das S; Kubota T; Song M; Daniel R; Berry-Kravis EM; Prior TW; Popovich B; Rosser L; Arinami T; Ledbetter DH Methylation analysis of the fragile X syndrome by PCR | 2 | 3 |
| 1588 | 5 | 8 | 1588 1997 HOSPITAL PRACTICE 32(4):73-& Warren ST Trinucleotide repetition and fragile X syndrome | 3 | 5 |
| 1589 | 11 | 15 | 1589 1997 HUMAN GENETICS 99(3):308-311 Willemsen R; Smits A; Mohkamsing S; vanBeerendonk H; deHaan A; deVries B; vandenOuweland A; Sistermans E; Galjaard H; Oostra BA Rapid antibody test for diagnosing fragile X syndrome: A validation of the technique | 34 | 41 |
| 1590 | 15 | 64 | 1590 1997 HUMAN GENETICS 100(3-4):407-414 Lavedan CN; Garrett L; Nussbaum RL Trinucleotide repeats (CGG)(22)TGG(CGG)(43)TGG(CGG)(21) from the fragile X gene remain stable in transgenic mice | 9 | 19 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1591 | 14 | 19 | 1591 1997 HUMAN GENETICS 100(5-6):564-568 Larsen LA; Gronskov K; NorgaardPedersen B; BrondumNielsen K; Hasholt L; Vuust J High-throughput analysis of fragile X (CGG)(n) alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresis | 5 | 23 |
| 1592 | 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 |
| 1593 | 4 | 22 | 1593 1997 HUMAN HEREDITY 47(5):254-262 Gurling HMD; Bolton PF; Vincent J; Melmer G; Rutter M Molecular and cytogenetic investigations of the fragile X region including the Frax A and Frax E CGG trinucleotide repeat sequences in families multiplex for autism and related phenotypes | 0 | 7 |
| 1594 | 21 | 35 | 1594 1997 HUMAN MOLECULAR GENETICS 6(7):971-979 Moutou C; Vincent MC; Biancalana V; Mandel JL Transition from premutation to full mutation in fragile X syndrome is likely to be prezygotic | 18 | 33 |
| 1595 | 12 | 38 | 1595 1997 HUMAN MOLECULAR GENETICS 6(9):1465-1472 Corbin F; Bouillon M; Fortin A; Morin S; Rousseau F; Khandjian EW The fragile X mental retardation protein is associated with poly(A)(+) mRNA in actively translating polyribosomes | 55 | 85 |
| 1596 | 18 | 64 | 1596 1997 HUMAN MOLECULAR GENETICS 6(11):1791-1801 Stoger R; Kajimura TM; Brown WT; Laird CD Epigenetic variation illustrated by DNA methylation patterns of the fragile-X gene FMR1 | 12 | 36 |
| 1597 | 26 | 38 | 1597 1997 HUMAN MUTATION 10(5):393-399 Wang YC; Lin ML; Lin SJ; Li YC; Li SY Novel point mutation within intron 10 of FMR-1 gene causing fragile X syndrome | 6 | 9 |
| 1598 | 51 | 134 | 1598 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 |
| 1599 | 24 | 61 | 1599 1997 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 27(4):415-435 Mazzocco MMM; Kates WR; Baumgardner TL; Freund LS; Reiss AL Autistic behaviors among girls with fragile X syndrome | 19 | 24 |
| 1600 | 21 | 51 | 1600 1997 JOURNAL OF CLINICAL INVESTIGATION 100(2):331-338 Jakala P; Hanninen T; Ryynanen M; Laakso M; Partanen K; Mannermaa A; Soininen H Fragile-X: Neuropsychological test performance, CGG triplet repeat lengths, and hippocampal volumes | 12 | 19 |
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