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Journal Abstract Search

586 related items for PubMed ID: 10631922

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  • 2. Multiorgan autoimmunity in a Turner syndrome patient with partial monosomy 2q and trisomy 10p.
    Grossi A, Palma A, Zanni G, Novelli A, Loddo S, Cappa M, Fierabracci A.
    Gene; 2013 Feb 25; 515(2):439-43. PubMed ID: 23262341
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  • 8. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS, Kamel AK, Helmy NA.
    Genet Couns; 2008 Feb 25; 19(2):199-209. PubMed ID: 18618995
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  • 10. Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14).
    Gentile M, Buonadonna AL, Cariola F, Fiorente P, Valenzano MC, Guanti G.
    J Med Genet; 1999 Jan 25; 36(1):77-82. PubMed ID: 9950374
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  • 11. [Trisomy of the short arm of chromosome 10p; description of a female patient with de novo duplication 10p11.2-15].
    Fechtrup B, Kalhoff H, Diekmann L, Fritz B.
    Klin Padiatr; 2000 Jan 25; 212(1):35-40. PubMed ID: 10719682
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  • 12. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
    Tüysüz B, Hacihanefioglu S, Silahtaroglu A, Yilmaz S, Deviren A, Cenani A.
    Genet Couns; 2000 Jan 25; 11(4):355-61. PubMed ID: 11140413
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  • 17. [46,XX/46,XX,del (10) (p13)/47,XX,+r/47,XX,del (10) (p13), + r mosaicism and partial trisomy 10p phenotype (author's transl)].
    Turleau C, Rethoré MO, Junien C, Lejeune J, de Grouchy J.
    Ann Genet; 1979 Jan 25; 22(3):178-81. PubMed ID: 316677
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  • 18. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
    Hegmann KM, Spikes AS, Orr-Urtreger A, Shaffer LG.
    Am J Med Genet; 1996 Jan 02; 61(1):10-5. PubMed ID: 8741910
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