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Journal Abstract Search

244 related items for PubMed ID: 3807920

  • 1. [Clinical picture of partial monosomy of chromosome 11 q].
    Dörr U.
    Monatsschr Kinderheilkd; 1986 Nov; 134(11):808-11. PubMed ID: 3807920
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  • 6. Partial monosomy of chromosome 2. Delineable syndrome of deletion 2 (q23-q31).
    Shabtai F, Klar D, Halbrecht I.
    Ann Genet; 1982 Nov; 25(3):156-8. PubMed ID: 6982665
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  • 10. [Wolf syndrome. Apropos of 2 cases].
    García González P, Pedraz García C, Merino Marcos L, Salazar Veloz J, Escudero Bueno G, Salazar Villalobos V.
    An Esp Pediatr; 1983 Feb; 18(2):113-7. PubMed ID: 6881733
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  • 12. Partial trisomy 8p (8p11.2-->pTER) and deletion of 13q (13q32-->qTER): case report.
    Yeşilyurt A, Dilli D, Oguz S, Dilmen U, Altug N, Candemir Z.
    Genet Couns; 2011 Feb; 22(1):35-40. PubMed ID: 21614986
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  • 13. De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delay.
    Chen CP, Lin SP, Chern SR, Lee CC, Huang JK, Wang W, Liao YW.
    Genet Couns; 2004 Feb; 15(4):437-42. PubMed ID: 15658619
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  • 15. Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q.
    Koiffmann CP, Gonzalez CH, Vianna-Morgante AM, Kim CA, Odone-Filho V, Wajntal A.
    Am J Med Genet; 1995 Jul 31; 58(1):46-9. PubMed ID: 7573155
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  • 17. [The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases].
    Destiné ML, Punnett HH, Thovichit S, DiGeorge AM, Weiss L.
    Ann Genet; 1967 Jun 31; 10(2):65-9. PubMed ID: 5298975
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  • 18. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J, Plaza J, Geán E.
    An Esp Pediatr; 1981 Nov 31; 15(5):469-73. PubMed ID: 7332149
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