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 *

293 related articles for article (PubMed ID: 6684008)

  • 1. The strength of association between fragile (X) chromosome presence and mental retardation.
    Silverman W; Lubin R; Jenkins EC; Brown WT
    Clin Genet; 1983 Jun; 23(6):436-40. PubMed ID: 6684008
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Is there a fragile(X) negative Martin-Bell syndrome?
    Thode A; Laing S; Partington MW; Turner G
    Am J Med Genet; 1988; 30(1-2):459-71. PubMed ID: 3052069
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Further evidence for genetic heterogeneity in the fragile X syndrome.
    Brown WT; Jenkins EC; Gross AC; Chan CB; Krawczun MS; Duncan CJ; Sklower SL; Fisch GS
    Hum Genet; 1987 Apr; 75(4):311-21. PubMed ID: 2883105
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Familial mental retardation and the fragile X syndrome].
    Veenema H; Pelckmans AJ; Geraedts JP; Van Leeuwen I; Zvelebil N
    Tijdschr Kindergeneeskd; 1984 Feb; 52(1):9-15. PubMed ID: 6585033
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fragile X syndrome: a major cause of X-linked mental retardation.
    Butler MG
    Compr Ther; 1988 Jul; 14(7):3-7. PubMed ID: 3060303
    [No Abstract]   [Full Text] [Related]  

  • 6. Fragile X chromosome in institutionalized male adults with mental retardation.
    Aoi T; Takashima H; Takada T; Okada T
    Keio J Med; 1989 Mar; 38(1):36-9. PubMed ID: 2785613
    [TBL] [Abstract][Full Text] [Related]  

  • 7. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3.
    Goonewardena P; Dahl N; Gustavson KH; Holmgren G; Pettersson U
    Ups J Med Sci Suppl; 1987; 44():155-64. PubMed ID: 2895524
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study.
    Blomquist HK; Gustavson KH; Holmgren G; Nordenson I; Pålsson-Stråe U
    Clin Genet; 1983 Dec; 24(6):393-8. PubMed ID: 6652951
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Linkage analysis of X-linked mental retardation with and without fragile-X using factor IX gene probe.
    Choo KH; George D; Filby G; Halliday JL; Leversha M; Webb G; Danks DM
    Lancet; 1984 Aug; 2(8398):349. PubMed ID: 6146889
    [No Abstract]   [Full Text] [Related]  

  • 10. Screening developmentally disabled male populations for fragile X: the effect of sample size.
    Fisch GS; Cohen IL; Jenkins EC; Brown WT
    Am J Med Genet; 1988; 30(1-2):655-63. PubMed ID: 3052070
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Bibliography on X-linked mental retardation, the fragile X and related subjects IV (1988).
    Spano LM; Opitz JM
    Am J Med Genet; 1988; 30(1-2):31-60. PubMed ID: 3052063
    [No Abstract]   [Full Text] [Related]  

  • 12. A variant of the fra(X) syndrome.
    Bühler EM; Hadziselimovic F; Pira U
    Hum Genet; 1982; 61(3):273-5. PubMed ID: 6890944
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Frequency of the fragile X syndrome in Japanese mentally retarded males.
    Arinami T; Kondo I; Nakajima S
    Hum Genet; 1986 Aug; 73(4):309-12. PubMed ID: 3744362
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The fragile X syndrome.
    Brown WT
    Neurol Clin; 1989 Feb; 7(1):107-21. PubMed ID: 2646518
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Dermatoglyphic peculiarities in families with X-linked mental retardation and fragile site Xq27: a collaborative study.
    Rodewald A; Froster-Iskenius U; Käb E; Langenbeck U; Schinzel A; Schmidt A; Schwinger E; Steinbach P; Veenema H; Wegner RD
    Clin Genet; 1986 Jul; 30(1):1-13. PubMed ID: 3757292
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Non-specific X-linked mental retardation: background, types, diagnosis and prevalence.
    Howard-Peebles PN
    J Ment Defic Res; 1982 Dec; 26 (Pt 4)():205-13. PubMed ID: 6763078
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An assessment of the use of flanking DNA markers for fra(X) syndrome carrier detection and prenatal diagnosis.
    Forster-Gibson CJ; Mulligan LM; Simpson NE; White BN; Holden JJ
    Am J Med Genet; 1986; 23(1-2):665-83. PubMed ID: 3006491
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Frequency of the fragile X syndrome in institutionalized mentally retarded females in Japan.
    Arinami T; Kondo I; Nakajima S; Hamaguchi H
    Hum Genet; 1987 Aug; 76(4):344-7. PubMed ID: 3610153
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Normal male carriers in the fra(X) form of X-linked mental retardation (Martin-Bell syndrome).
    Froster-Iskenius U; McGillivray BC; Dill FJ; Hall JG; Herbst DS
    Am J Med Genet; 1986; 23(1-2):619-31. PubMed ID: 3953672
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Fragile (X) X-linked mental retardation. II. Frequency and replication pattern of fragile (X)(q28) in heterozygotes.
    Knoll JH; Chudley AE; Gerrard JW
    Am J Hum Genet; 1984 May; 36(3):640-5. PubMed ID: 6731439
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.