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Journal Abstract Search

217 related items for PubMed ID: 28981940

  • 1. [Prenatal genetic analysis of a fetus with Wolf-Hirschhorn syndrome and Edward syndrome].
    Shen X, He P, Fang R, Yao J, Li W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct 10; 34(5):714-717. PubMed ID: 28981940
    [Abstract] [Full Text] [Related]

  • 2. [A case of Wolf-Hirschhorn syndrome diagnosed by single nucleotide polymorphism array].
    Jin Y, Liu X, Li S, Zhou C, Liu X, Song Q, Wang L, Miao Z.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Aug 10; 33(4):501-4. PubMed ID: 27455007
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  • 3. [Prenatal diagnosis of three fetuses with small supernumerary marker chromosomes].
    Li W, Fang R, Shen X, Yao J, Xue J, Shen G.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Dec 10; 37(12):1344-1348. PubMed ID: 33306818
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  • 4. [Prenatal diagnosis for a pedigree affected with Wolf-Hirschhorn syndrome due to a subtle chromosomal translocation].
    Xing Y, Xiong S, Yuan M, Deng L, Zhou J, Zou G, Sun L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Jul 10; 36(7):682-685. PubMed ID: 31302910
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  • 6. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
    Zhu CJ, Huang ZY, Wu WQ, Zhao Q, Jiang HY, Xie JS.
    Zhonghua Er Ke Za Zhi; 2012 Jun 10; 50(6):460-4. PubMed ID: 22931946
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  • 8. [Improved identification for 5p deletion syndrome and partial trisomy 11q presented in a fetus by SNP array].
    Shi S, Pan G, Yang Y, Yan R, Li W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr 10; 33(2):195-9. PubMed ID: 27060314
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  • 9. [Prenatal diagnosis of a fetus with two small supernumerary marker chromosomes].
    Zhang J, Jiang Y, Cai M, Ge Y, Zhou Y, Wang W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Dec 10; 36(12):1222-1225. PubMed ID: 31813153
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  • 11. Detection of recurrent 4p16.3 microdeletion with 2p25.3 microduplication by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in a fetus from a family with Wolf-Hirschhorn syndrome.
    Yang WX, Pan H, Wang ST, Li L, Wu HR, Qi Y.
    Taiwan J Obstet Gynecol; 2016 Feb 10; 55(1):104-8. PubMed ID: 26927259
    [Abstract] [Full Text] [Related]

  • 12. [Prenatal diagnosis of a case with combined Wolf-Hirschhorn syndrome and Jacobsen syndrome].
    Dong Y, Hu H, Hu H, Zhang R, Hu B, Long Y, Xu G, Yao H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Aug 10; 32(4):512-4. PubMed ID: 26252097
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  • 15. [Phenotypic and genetic analysis of a boy with a 10p15.3 deletion and partial trisomy 18p syndrome].
    Zhang B, Kong J, Mei S, Li D, Song Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jul 10; 37(7):785-788. PubMed ID: 32619265
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  • 16. [Prenatal diagnosis of a case with 46,XX,del(4),dup(21)].
    Zhang L, Ren M, Song G, Liu X, Zhang J, Zhang X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb 10; 34(1):50-52. PubMed ID: 28186593
    [Abstract] [Full Text] [Related]

  • 17. [Application of single nucleotide polymorphism microarray and fluorescence in situ hybridization analysis for the prenatal diagnosis of a case with Pallister-Killian syndrome].
    Zhang W, Guo Z, Wang W, Sun Y, Zhang C, Wang X, Zhang L, Wang C.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr 10; 35(2):232-235. PubMed ID: 29652999
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