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Journal Abstract Search

289 related items for 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
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  • 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
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  • 4. Dermatoglyphic indices of males with the fragile X syndrome and of the female heterozygotes.
    Simpson NE.
    Am J Med Genet; 1986 Jul; 23(1-2):171-8. PubMed ID: 3953645
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  • 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
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  • 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
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  • 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
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  • 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 Aug; 30(1-2):177-83. PubMed ID: 3177443
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  • 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
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  • 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
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  • 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 Aug; 23(1-2):619-31. PubMed ID: 3953672
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  • 16. [Clinical, cytogenetic and molecular aspects of fragile X syndrome].
    Veenema H.
    Tijdschr Kindergeneeskd; 1989 Oct; 57(5):153-8. PubMed ID: 2683200
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  • 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
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  • 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
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