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Journal Abstract Search

95 related items for PubMed ID: 4220490

  • 1. Delayed ontogenesis in human trisomy syndromes.
    Hall B.
    Hereditas; 1965; 52(3):334-44. PubMed ID: 4220490
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  • 5. Trisomy No. 17-18. Report of two cases.
    Paerregaard P, Mikkelsen M, Froland A, Andersen H.
    Acta Pathol Microbiol Scand; 1966; 67(4):479-87. PubMed ID: 5924747
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  • 9. [Preliminary observations on 2 cases of trisomy 17-18].
    Giuffrè L, Liuzzo B.
    Minerva Pediatr; 1967 Nov 24; 19(47):2105-6. PubMed ID: 5606105
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  • 16. [Familial variant of the Y chromosome].
    Jeske J, Hübner H.
    Endokrynol Pol; 1970 Nov 24; 21(4):411-4. PubMed ID: 4248804
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  • 19. Loss of the extra chromosome 21 in a patient with Down syndrome and myelodysplasia.
    Tan D, Lau LC, Teng LM, Sane S, Lim TH, Tien SL.
    Cancer Genet Cytogenet; 2008 Jan 01; 180(1):79-82. PubMed ID: 18068540
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  • 20. [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 01; 21(3):187-206. PubMed ID: 4282490
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