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Journal Abstract Search

74 related items for PubMed ID: 1468637

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  • 2. The unbalanced offspring of the male carriers of the 11q;22q translocation: nondisjunction at meiosis II in a balanced spermatocyte.
    Simi P, Ceccarelli M, Barachini A, Floridia G, Zuffardi O.
    Hum Genet; 1992 Feb; 88(4):482-3. PubMed ID: 1740326
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  • 3. 11q;22q translocation: third case of imbalance not due to 3:1 nondisjunction in first meiosis.
    Lurie IW, Podleschuk LV.
    Am J Med Genet; 1992 Jan 15; 42(2):216. PubMed ID: 1733172
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  • 7. Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families.
    Schinzel A, Schmid W, Auf der Maur P, Moser H, Degenhardt KH, Geisler M, Grubisic A.
    Hum Genet; 1981 Jan 15; 56(3):249-62. PubMed ID: 7239508
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  • 8. Partial trisomy 22 with Dandy-Walker malformation.
    Katafuchi Y, Hashino K, Maeno Y, Komori H, Yamashita Y, Horikawa M, Abe K, Niikawa N, Kato H.
    Acta Paediatr Jpn; 1990 Oct 15; 32(5):566-70. PubMed ID: 2284936
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  • 9. Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis.
    Lockwood DH, Farrier A, Hecht F, Allanson J.
    Hum Genet; 1989 Oct 15; 83(3):287-8. PubMed ID: 2793173
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  • 10. Supernumerary chromosome marker Der(22)t(11;22) resulting from a maternal balanced translocation.
    Hou JW.
    Chang Gung Med J; 2003 Jan 15; 26(1):48-52. PubMed ID: 12656309
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  • 11. Tertiary trisomy (22q11q),47,+der(22),t(11;22).
    Biederman BM, Lin CC, Lowry RB, Somerville R.
    Hum Genet; 1980 Feb 15; 53(2):173-7. PubMed ID: 7358384
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  • 13. [Marker chromosomes as a product of familial translocation (11;22) identified with molecular cytogenetic methods].
    Stankiewicz P, Korniszewski L, Bocian E, Stańczak H.
    Pediatr Pol; 1996 Mar 15; 71(3):241-5. PubMed ID: 8966096
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  • 14. Unusual segregation for 11q;22q parental translocation.
    Allanson JE.
    Prenat Diagn; 1993 Sep 15; 13(9):889-91. PubMed ID: 8123159
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  • 15. Predisposition for breast cancer in carriers of constitutional translocation 11q;22q.
    Lindblom A, Sandelin K, Iselius L, Dumanski J, White I, Nordenskjöld M, Larsson C.
    Am J Hum Genet; 1994 May 15; 54(5):871-6. PubMed ID: 8178827
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  • 16. A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24).
    Balci S, Aypar E, Beksaç MS, Bartsch O.
    Genet Couns; 2009 May 15; 20(2):125-32. PubMed ID: 19650409
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  • 19. Duplication 11 (q22----qter) in an infant. A case report with review.
    Greig F, Rosenfeld W, Verma RS, Babu KA, David K.
    Ann Genet; 1985 May 15; 28(3):185-8. PubMed ID: 3879155
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