These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 1570846)

  • 1. Fragile-X syndrome: unique genetics of the heritable unstable element.
    Yu S; Mulley J; Loesch D; Turner G; Donnelly A; Gedeon A; Hillen D; Kremer E; Lynch M; Pritchard M
    Am J Hum Genet; 1992 May; 50(5):968-80. PubMed ID: 1570846
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Pathology of unstable sequence of genome: fragile-X-syndrome].
    Beldjord C; Richard L
    C R Seances Soc Biol Fil; 1992; 186(4):363-70. PubMed ID: 1301224
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n.
    Kremer EJ; Pritchard M; Lynch M; Yu S; Holman K; Baker E; Warren ST; Schlessinger D; Sutherland GR; Richards RI
    Science; 1991 Jun; 252(5013):1711-4. PubMed ID: 1675488
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Heritable unstable DNA sequences and hypermethylation associated with fragile X syndrome in Japanese families.
    Hori T; Yamauchi M; Seki N; Tsuji S; Kondo I
    Clin Genet; 1993 Jan; 43(1):34-8. PubMed ID: 8462194
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cytogenetic and molecular analysis of dynamic mutation associated with fragile X syndrome.
    Seki N; Ishikiriyama S; Yamauchi M; Hori T
    Jpn J Genet; 1994 Jun; 69(3):259-67. PubMed ID: 8080657
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular heterogeneity of the fragile X syndrome.
    Nakahori Y; Knight SJ; Holland J; Schwartz C; Roche A; Tarleton J; Wong S; Flint TJ; Froster-Iskenius U; Bentley D
    Nucleic Acids Res; 1991 Aug; 19(16):4355-9. PubMed ID: 1886762
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site.
    Richards RI; Holman K; Kozman H; Kremer E; Lynch M; Pritchard M; Yu S; Mulley J; Sutherland GR
    J Med Genet; 1991 Dec; 28(12):818-23. PubMed ID: 1757956
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.
    Fu YH; Kuhl DP; Pizzuti A; Pieretti M; Sutcliffe JS; Richards S; Verkerk AJ; Holden JJ; Fenwick RG; Warren ST
    Cell; 1991 Dec; 67(6):1047-58. PubMed ID: 1760838
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evidence of founder chromosomes in fragile X syndrome.
    Richards RI; Holman K; Friend K; Kremer E; Hillen D; Staples A; Brown WT; Goonewardena P; Tarleton J; Schwartz C
    Nat Genet; 1992 Jul; 1(4):257-60. PubMed ID: 1302021
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general population.
    Snow K; Doud LK; Hagerman R; Pergolizzi RG; Erster SH; Thibodeau SN
    Am J Hum Genet; 1993 Dec; 53(6):1217-28. PubMed ID: 7902673
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genotype mosaicism in fragile X fetal tissues.
    Wöhrle D; Hirst MC; Kennerknecht I; Davies KE; Steinbach P
    Hum Genet; 1992 Apr; 89(1):114-6. PubMed ID: 1349561
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Polymerase chain reaction analysis of fragile X mutations.
    Erster SH; Brown WT; Goonewardena P; Dobkin CS; Jenkins EC; Pergolizzi RG
    Hum Genet; 1992; 90(1-2):55-61. PubMed ID: 1427787
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fragile X syndrome without CCG amplification has an FMR1 deletion.
    Gedeon AK; Baker E; Robinson H; Partington MW; Gross B; Manca A; Korn B; Poustka A; Yu S; Sutherland GR
    Nat Genet; 1992 Aug; 1(5):341-4. PubMed ID: 1302032
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis of fragile X syndrome by direct detection of the dynamic mutation due to an unstable DNA sequence.
    Yamauchi M; Nagata S; Seki N; Toyama Y; Harada N; Niikawa N; Masuno I; Kajii T; Hori T
    Clin Genet; 1993 Oct; 44(4):169-72. PubMed ID: 8261644
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Fragile X syndrome.
    Laxova R
    Adv Pediatr; 1994; 41():305-42. PubMed ID: 7992687
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Unstable DNA sequence and methylation in fragile X syndrome].
    Fu SD; Shen Y; Fan Y
    Zhonghua Yi Xue Za Zhi; 1994 Oct; 74(10):611-4, 646-7. PubMed ID: 7842338
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation.
    Heitz D; Devys D; Imbert G; Kretz C; Mandel JL
    J Med Genet; 1992 Nov; 29(11):794-801. PubMed ID: 1453430
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fragile X syndrome unstable element, p(CCG)n, and other simple tandem repeat sequences are binding sites for specific nuclear proteins.
    Richards RI; Holman K; Yu S; Sutherland GR
    Hum Mol Genet; 1993 Sep; 2(9):1429-35. PubMed ID: 8242066
    [TBL] [Abstract][Full Text] [Related]  

  • 19. FRAXE and mental retardation.
    Mulley JC; Yu S; Loesch DZ; Hay DA; Donnelly A; Gedeon AK; Carbonell P; López I; Glover G; Gabarrón I
    J Med Genet; 1995 Mar; 32(3):162-9. PubMed ID: 7783162
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Instability of the CGG repeat at the FRAXA locus and variable phenotypic expression in a large fragile X pedigree.
    Pintado E; de Diego Y; Hmadcha A; Carrasco M; Sierra J; Lucas M
    J Med Genet; 1995 Nov; 32(11):907-8. PubMed ID: 8592340
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.