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Journal Abstract Search

189 related items for PubMed ID: 5519607

  • 21.
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  • 22. Paternal transmission of a B-D translocation, t(4p-; 14p + or 15p+), resulting in a partial 4p trisomy.
    Gouw WL, Anders GJ, ten Kate LP, de Groot CJ.
    Humangenetik; 1972; 16(3):251-9. PubMed ID: 5082106
    [No Abstract] [Full Text] [Related]

  • 23. Inherited pericentric inversion of chromosome no. 4.
    Wilson MG, Towner JW, Coffin GS, Forsman I.
    Am J Hum Genet; 1970 Nov; 22(6):679-90. PubMed ID: 5518460
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  • 24.
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  • 25. Partial trisomy 12q24.31----qter.
    Tajara EH, Varella-Garcia M, Gusson AC.
    J Med Genet; 1985 Feb; 22(1):73-6. PubMed ID: 3981585
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  • 26.
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  • 27. Malformative syndrome with ring chromosome 13.
    Fryns JP, Deoover J, Van den Berghe H.
    Humangenetik; 1974 Feb; 24(3):235-40. PubMed ID: 4140834
    [No Abstract] [Full Text] [Related]

  • 28.
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  • 30. A 13-year-old girl with Wolf's syndrome and karyotype 46,XX,del(4)(pter integral p15::p12 integral qter),9qh+. Increased risk of structural chromosome abnormalities in the progeny of mothers with 9qh+.
    Nielsen J, Fischer O, Rasmussen K, Sillesen I, Bernsen A, Saldaña-Garcia P.
    J Ment Defic Res; 1977 Jun; 21(2):119-26. PubMed ID: 894706
    [No Abstract] [Full Text] [Related]

  • 31.
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  • 32. A girl with Wolf-Hirschorn syndrome and mosaicism 46,XX-46,XX,4p-.
    Judge CG, Garson OM, Pitt DB, Sutherland GR.
    J Ment Defic Res; 1974 Mar; 18(0):79-85. PubMed ID: 4423845
    [No Abstract] [Full Text] [Related]

  • 33. A case of a girl with a 21 ring chromosome.
    Kucerová M, Polívková Z.
    Hum Hered; 1974 Mar; 24(1):100-4. PubMed ID: 4136482
    [No Abstract] [Full Text] [Related]

  • 34.
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  • 35. Microcephaly, mental retardation and hypertelorism in chromosome deletion studies.
    Miller JQ.
    Neurology; 1973 Nov; 23(11):1141-6. PubMed ID: 4795737
    [No Abstract] [Full Text] [Related]

  • 36. Deletion of the short arm of chromosome No. 10.
    Shokeir MH, Ray M, Hamerton JL, Bauder F, O'Brien H.
    J Med Genet; 1975 Mar; 12(1):99-103. PubMed ID: 47396
    [Abstract] [Full Text] [Related]

  • 37. Human congenital abnormalities associated with a long group B chromosome.
    Holden HE.
    J Hered; 1971 Mar; 62(6):380-1. PubMed ID: 5137684
    [No Abstract] [Full Text] [Related]

  • 38. Ring chromosome 8 in a boy with multiple congenital abnormalities and mental retardation.
    Hamers AJ, van Kempen C.
    J Med Genet; 1977 Dec; 14(6):451-5. PubMed ID: 604497
    [Abstract] [Full Text] [Related]

  • 39.
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  • 40.
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