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Journal Abstract Search

176 related items for PubMed ID: 24737738

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  • 26. A Familial Small Supernumerary Marker Chromosome 15 Associated with Cryptic Mosaicism with Two Different Additional Marker Chromosomes Derived de novo from Chromosome 9: Detailed Case Study and Implications for Recurrent Pregnancy Loss.
    Čulić V, Lasan-Trcić R, Liehr T, Lebedev IN, Pivić M, Pavelic J, Vulić R.
    Cytogenet Genome Res; 2018; 156(4):179-184. PubMed ID: 30466092
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  • 27. Meiotic segregation analysis by FISH investigation of spermatozoa of a 46,Y,der(X),t(X;Y)(qter-->p22::q11-->qter) carrier.
    Morel F, Fellmann F, Roux C, Bresson JL.
    Cytogenet Cell Genet; 2001; 92(1-2):63-8. PubMed ID: 11306798
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  • 28. 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; 83(3):287-8. PubMed ID: 2793173
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  • 29. A dysmorphic newborn with 45,X,der(1)inv(1)(p13;qter)t(Y;1)(pter-->q11;p13),-Y de novo karyotype.
    Tatar A, Oztas S, Yakut T, Ors R.
    Genet Couns; 2005 Oct; 16(2):173-7. PubMed ID: 16080298
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  • 35. Prenatal diagnosis of the maternal derivative chromosome der(15)t(Y;15)(q12;p13) in a dizygotic twin pregnancy.
    Chen PY, Yen JH, Cheng CF, Chen PC, Li YS, Li TY, Yeh CN, Fang JS.
    Tzu Chi Med J; 2016 Oct; 28(4):176-179. PubMed ID: 28757753
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  • 36. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY.
    Am J Med Genet; 1994 Nov 01; 53(2):108-40. PubMed ID: 7856637
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  • 38. [Genetic diagnosis and follow up of a fetus with Emanuel syndrome].
    Zhao Y, Pang H, Gao M, Feng X, Guan Y, Zhao H, Tong D, Hua J, Cao X, He S, Li-Ling J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct 10; 34(5):709-713. PubMed ID: 28981939
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  • 39. Two cases of complex balanced autosomal translocations associated with severe oligozoospermia.
    Sha YW, Mei LB, Ji ZY, Ding L, Ge Y, Wu Q, Kong H, Su ZY, Li P.
    Gene; 2018 Jul 15; 663():126-130. PubMed ID: 29684482
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  • 40. Characterization of chromosomal breakpoints in an ALL patient using cross-species color banding.
    Koo SH, Kwon KC, Park JW, Lee YE, Kim JW.
    Cancer Genet Cytogenet; 2000 Jun 15; 119(2):118-20. PubMed ID: 10867146
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