BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

293 related articles for article (PubMed ID: 3978845)

  • 1. Dermatoglyphic findings in patients with fragile X-chromosome.
    Hirth L; Singh S; Schilling S; Müller E; Goedde HW
    Clin Genet; 1985 Feb; 27(2):118-21. PubMed ID: 3978845
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Fragile-X syndrome III: dermatoglyphic studies in males.
    Simpson NE; Newman BJ; Partington MW
    Am J Med Genet; 1984 Jan; 17(1):195-207. PubMed ID: 6711595
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Dermatoglyphic indices of males with the fragile X syndrome and of the female heterozygotes.
    Simpson NE
    Am J Med Genet; 1986; 23(1-2):171-8. PubMed ID: 3953645
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Discriminant analysis of dermatoglyphic measurements in fragile X males and females.
    Loesch DZ
    Clin Genet; 1988 Mar; 33(3):169-75. PubMed ID: 3359677
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. Fragile X trait in a large kindred: transmission also through normal males.
    Van Roy BC; De Smedt MC; Raes RA; Dumon JE; Leroy JG
    J Med Genet; 1983 Aug; 20(4):286-9. PubMed ID: 6620329
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dermatoglyphic findings in fragile X syndrome: a causal hypothesis points to X-Y interchange.
    Loesch DZ
    Ann Hum Genet; 1986 Oct; 50(4):385-98. PubMed ID: 3442405
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A dermatoglyphic study of a group of Sicilian children with fragile-X syndrome.
    Milone G; Conti L; Rizzo R; Sanfilippo S; Sammito V; Romano C
    Am J Med Genet; 1988; 30(1-2):177-83. PubMed ID: 3177443
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Children with the fragile X chromosome at schools for the mildly mentally retarded.
    Thake A; Todd J; Webb T; Bundey S
    Dev Med Child Neurol; 1987 Dec; 29(6):711-9. PubMed ID: 3691971
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Fragile X chromosome: clinical and cytogenetic studies on cases from seven families.
    McDermott A; Walters R; Howell RT; Gardner A
    J Med Genet; 1983 Jun; 20(3):169-78. PubMed ID: 6876108
    [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. Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardation.
    Voelckel MA; Mattei MG; N'Guyen C; Philip N; Birg F; Mattei JF
    Hum Genet; 1988 Dec; 80(4):375-8. PubMed ID: 2904402
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [Clinical, cytogenetic and molecular aspects of fragile X syndrome].
    Veenema H
    Tijdschr Kindergeneeskd; 1989 Oct; 57(5):153-8. PubMed ID: 2683200
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Institutional screening for the fragile X syndrome.
    Hagerman R; Berry R; Jackson AW; Campbell J; Smith AC; McGavran L
    Am J Dis Child; 1988 Nov; 142(11):1216-21. PubMed ID: 3177330
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. A cytogenetic study of a population of retarded females with special reference to the fragile (X) syndrome.
    Mayer M; Abruzzo MA; Jacobs PA; Yee SC
    Hum Genet; 1985; 69(3):206-8. PubMed ID: 3980014
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A 15-item checklist for screening mentally retarded males for the fragile X syndrome.
    Butler MG; Mangrum T; Gupta R; Singh DN
    Clin Genet; 1991 May; 39(5):347-54. PubMed ID: 1860251
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.