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Journal Abstract Search

113 related items for PubMed ID: 4140322

  • 21. [Double aneuploidy: 46,XX-45,XO-47,XX,G+. Case report].
    Grosse KP, Hopfengärtner F, Schwanitz G.
    Humangenetik; 1971; 13(4):333-7. PubMed ID: 4257570
    [No Abstract] [Full Text] [Related]

  • 22. [Dermatoglyphics and genetic disorders].
    Kahn-Koopman H.
    Ned Tijdschr Geneeskd; 1972 Nov 18; 116(47):2141-6. PubMed ID: 4264374
    [No Abstract] [Full Text] [Related]

  • 23. [DERMATOGLYPHIC CHANGES IN DYSGENETIC STATES].
    DE ALMEIDA JC, BARCINSKI M, ABREUMDO D, POVOA LC.
    Arq Bras Endocrinol Metabol; 1963 Dec 18; 12():177-91. PubMed ID: 14164198
    [No Abstract] [Full Text] [Related]

  • 24. [Down's syndrome with confirmation of trisomy G solely in fibroblast cultures].
    Haberlandt W.
    J Genet Hum; 1973 Sep 18; 21(3):215-22. PubMed ID: 4282491
    [No Abstract] [Full Text] [Related]

  • 25. [Peculiarities of dermatoglyphics in chromosomal diseases].
    Verlinskaia DK, Shtil'bans II.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1966 Sep 18; 66(11):1608-13. PubMed ID: 4234112
    [No Abstract] [Full Text] [Related]

  • 26. Letter: Mongolism by tertiary trisomy.
    Chaganti RS, Morillo-Cucci G, Degnan M, German J.
    Lancet; 1975 Mar 22; 1(7908):698-9. PubMed ID: 47133
    [No Abstract] [Full Text] [Related]

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  • 28. [Down's syndrome with predominantly normal karyotype in lymphocyte culture but extensive G trisomy in fibroblast culture].
    Haberlandt W, Wunderlich C.
    Arztl Forsch; 1972 Sep 10; 26(9):309-16. PubMed ID: 4262890
    [No Abstract] [Full Text] [Related]

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  • 30. [Progeny of mothers with trisomy 21 (apropos of a case)].
    Van De Velde-Staquet MF, Breynaert R, Walbaum R, Saint-Aubert P, Farriaux JP, Fontaine G.
    J Genet Hum; 1973 Sep 10; 21(3):187-206. PubMed ID: 4282490
    [No Abstract] [Full Text] [Related]

  • 31. Down syndrome with trisomy in one triplet.
    Shiono H, Kadowaki JI, Tsuneta H, Nagai B, Nanbu H.
    Am J Dis Child; 1977 May 10; 131(5):522-4. PubMed ID: 140603
    [Abstract] [Full Text] [Related]

  • 32. [t(7q-; 21q-plus) and familial and trisomy 21].
    Giraud F, Hartung M, Mattei JF, Mattie MG.
    Ann Genet; 1974 Mar 10; 17(1):49-53. PubMed ID: 4276449
    [No Abstract] [Full Text] [Related]

  • 33. A new case of incomplete Down syndrome with partial trisomy 21.
    Giorgi PL, Paci A, Ceccarelli M, Vizzoni L.
    Helv Paediatr Acta; 1968 Oct 10; 23(5):540-5. PubMed ID: 4238457
    [No Abstract] [Full Text] [Related]

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  • 40. [Significance of the type of chromosome aberrations and biochemical disorders for diagnosis of Down's syndrome and the phenotype of partial trisomy 21].
    Mikiel-Kostyra K, Czerski P, Bartosz G, Sito A, Leyka W.
    Pediatr Pol; 1980 Jan 10; 55(1):23-32. PubMed ID: 6445053
    [No Abstract] [Full Text] [Related]

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