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Journal Abstract Search

188 related items for PubMed ID: 6215327

  • 1. Macroorchidism and fragile X in mentally retarded males. Clinical, cytogenetic, and some hormonal investigations in mentally retarded males, including two with the fragile site at Xq28, fra(X)(q28).
    Nielsen KB, Tommerup N, Dyggve HV, Schou C.
    Hum Genet; 1982; 61(2):113-7. PubMed ID: 6215327
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  • 3. [Sex linked mental deficiency, unusual facies, macroorchidism and fragile site on chromosome X (author's transl)].
    Turleau C, Czernichow P, Gorin R, Royer P, de Grouchy J.
    Ann Genet; 1979; 22(4):205-9. PubMed ID: 317781
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  • 7. Martin-Bell syndrome fra(X) (q28) in a Sri Lankan family.
    Soysa P, Senanayahe M, Mikkelsen M, Poulsen H.
    J Ment Defic Res; 1982 Dec; 26 (Pt 4)():251-7. PubMed ID: 7169632
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  • 9. The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.
    Veenema H, Carpenter NJ, Bakker E, Hofker MH, Ward AM, Pearson PL.
    J Med Genet; 1987 Jul; 24(7):413-21. PubMed ID: 2886667
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  • 10. Fragile X screening program in New York State.
    Nolin SL, Snider DA, Jenkins EC, Brown WT, Krawczun M, Stetka D, Houck G, Dobkin CS, Strong G, Smith-Dobransky G.
    Am J Med Genet; 1991 Jul; 38(2-3):251-5. PubMed ID: 2018068
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  • 12. [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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  • 13. Fragile-X mutation and Klinefelter syndrome: a reappraisal.
    Filippi G, Pecile V, Rinaldi A, Siniscalco M.
    Am J Med Genet; 1988 Oct; 30(1-2):99-107. PubMed ID: 3177482
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  • 14. 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
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  • 17. 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
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  • 19. 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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