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Journal Abstract Search

176 related items for PubMed ID: 24737738

  • 1. 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; 164A(8):2048-53. PubMed ID: 24737738
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  • 2. Mosaicism for Robertsonian jumping translocation at amniocentesis: 45,XY,der(15;22)(q10;q10)mat/46,XY,i(15)(q10)/46,XY, genetic counseling, prenatal diagnosis and postnatal follow-up in a pregnancy with a favorable fetal outcome.
    Chen CP, Tseng JJ, Wu FT, Pan YT, Wu PS, Chern SR, Lee CC, Wang W.
    Taiwan J Obstet Gynecol; 2023 Jul; 62(4):588-593. PubMed ID: 37407201
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  • 3. [Report on 16 rare species of human chromosomal].
    Han WT, Wang G, Jiang M, Zhang ZF, Liu GX, Wang CX, Bian CY, Yu P.
    Yi Chuan; 2005 Mar; 27(2):201-4. PubMed ID: 15843345
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  • 4. 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; 105(2):226-229. PubMed ID: 27686674
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  • 5. Prenatal diagnosis of jumping translocation involving chromosome 22 with ultrasonographic findings.
    Aslan H, Karaman B, Yildirim G, Ceylan Y.
    Prenat Diagn; 2005 Nov; 25(11):1024-7. PubMed ID: 16231308
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  • 6. 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 Nov; 93(3-4):168-70. PubMed ID: 11528107
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  • 7. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3.
    Chen CP, Ko TM, Chen CY, Chern SR, Wu PS, Chen SW, Wu FT, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2019 Nov; 58(6):864-868. PubMed ID: 31759544
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  • 8. Two new chromosomal abnormalities in chronic myelogenous leukemia 46,XY,t(9;15;22)(q34;q22;q11) and 46,XY,t(6;9;12;22)(p21;q34;q24;q11).
    Ramirez GM, Macera MJ, Verma RS.
    Cancer Genet Cytogenet; 1989 Mar; 38(1):115-9. PubMed ID: 2713807
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  • 10. Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.
    Armstrong SJ, Goldman AS, Speed RM, Hultén MA.
    Am J Hum Genet; 2000 Sep; 67(3):601-9. PubMed ID: 10936106
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  • 15. Prenatal diagnosis and molecular cytogenetic analyses of a homozygous Robertsonian translocation family with novel mosaic Robertsonian fission karyotype.
    Xu Z, Luo H, Li M, OuYang L, Xia Z.
    Psychiatr Genet; 2024 Oct 01; 34(5):106-110. PubMed ID: 39248081
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  • 16. Familial complex chromosome rearrangement ascertained by in situ hybridisation.
    Fuster C, Miguez L, Miró R, Rigola MA, Perez A, Egozcue J.
    J Med Genet; 1997 Feb 01; 34(2):164-6. PubMed ID: 9039997
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  • 17. [Application of combined fluorescence in situ hybridization and karyotype analysis for the diagnosis of Robertsonian translocation type trisomy 21].
    Zhang WG, Zhang WQ, Dai MZ, Chen XJ, Zhang Y, Zheng R.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Apr 01; 30(2):210-3. PubMed ID: 23568738
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