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Journal Abstract Search

168 related items for PubMed ID: 2793173

  • 21. Prenatal diagnosis of supernumerary chromosome derivative (22) due to maternal balanced translocation in association with diaphragmatic hernia: a case report.
    Kadir RA, Hastings R, Economides DL.
    Prenat Diagn; 1997 Aug; 17(8):761-4. PubMed ID: 9267900
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  • 22. Unusual chromosomal mosaicism as a cause of mental retardation and congenital malformations in a familial reciprocal translocation carrier, t(17;22)(q24.2;q11.23).
    Dufke A, Mayrhofer H, Enders H, Kaiser P, Leipoldt M.
    Cytogenet Cell Genet; 2001 Aug; 93(3-4):168-70. PubMed ID: 11528107
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  • 24. Unusual mosaic karyotype resulting from adjacent 1 segregation of t(11;22): importance of performing skin fibroblast karyotype in patients with unexplained multiple congenital anomalies.
    Kulharya AS, Lovell CM, Flannery DB.
    Am J Med Genet; 2002 Dec 15; 113(4):367-70. PubMed ID: 12457409
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  • 26. Constitutional t(8;22)(q24;q11.2) that mimics the variant Burkitt-type translocation in Philadelphia chromosome-positive chronic myeloid leukemia.
    Kawamoto S, Yamamoto K, Toyoda M, Yakushijin K, Matsuoka H, Minami H.
    Int J Hematol; 2017 Feb 15; 105(2):226-229. PubMed ID: 27686674
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  • 27. 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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  • 30. Involvement of 3:1 disjunction in the common reciprocal translocation t(11;22) (q23.3;q11.2).
    Chandley AC.
    Hum Genet; 1992 Jan 15; 90(1-2):191-2. PubMed ID: 1427783
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  • 33. Meiotic segregation in familial reciprocal translocation t(8q;22q).
    Gödde-Salz E, Oesinghaus S, Grote W.
    Am J Med Genet; 1982 Feb 15; 11(2):241-7. PubMed ID: 7065009
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  • 35. Malignant rhabdoid tumor of the kidney: involvement of chromosome 22.
    Shashi V, Lovell MA, von Kap-herr C, Waldron P, Golden WL.
    Genes Chromosomes Cancer; 1994 May 15; 10(1):49-54. PubMed ID: 7519873
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  • 36. Distinct karyotypes in two offspring of a man with jumping translocation karyotype 45,XY,der(16)t(16;22)(q24;q11.2), -22 [59]/45,XY,der(1)t(1;22)(p36;q11.2), -22 [11]/45,XY,der(22)t(22;22)(p13;q11.2), -22 [10].
    Hu H, Yao H, Dong Y, Long Y, Xu L, Hu B, Xu G, Liang Z.
    Am J Med Genet A; 2014 Aug 15; 164A(8):2048-53. PubMed ID: 24737738
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  • 40. Molecular cytogenetic characterization of a familial balanced reciprocal translocation t(11;18) (q13.3; q23) associated with pregnancy wastage.
    Liu JY, Wang XR, Zeng XL, Zhang CS, Hao S, Song YC.
    Cytogenet Genome Res; 2003 Aug 15; 103(1-2):8-13. PubMed ID: 15004456
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