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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

217 related items for PubMed ID: 28981940

  • 21. 4p16.3 microdeletions and microduplications detected by chromosomal microarray analysis: New insights into mechanisms and critical regions.
    Bi W, Cheung SW, Breman AM, Bacino CA.
    Am J Med Genet A; 2016 Oct; 170(10):2540-50. PubMed ID: 27287194
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  • 24. [Genetic analysis of a child with mental retardation and hypospadia].
    Ma N, Pang J, Peng Y, Jia Z, Xi H, Liu G, Zhou Y, Wang H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Dec 10; 36(12):1199-1202. PubMed ID: 31813147
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  • 25. [Cytogenetic and molecular genetic analysis of small supernumerary marker chromosomes in fetal amniotic fluid].
    Zhang W, Pan Y, Zhang Y, Dai M, Chen X, Shi W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr 10; 34(2):187-191. PubMed ID: 28397215
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  • 27. Prenatal diagnosis of Wolf-Hirschhorn syndrome: from ultrasound findings, diagnostic technology to genetic counseling.
    Xing Y, Holder JL, Liu Y, Yuan M, Sun Q, Qu X, Deng L, Zhou J, Yang Y, Guo M, Cheung SW, Sun L.
    Arch Gynecol Obstet; 2018 Aug 10; 298(2):289-295. PubMed ID: 29808250
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  • 29. [Prenatal diagnosis of Jacobsen syndrome in a fetus carried by a pregnant woman with intellectual disability].
    Guo C, Wang J, Tang Y, Shi H, Liu J, Zhao L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Aug 10; 36(8):826-288. PubMed ID: 31400138
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  • 31. [Prenatal diagnosis of a fetus with 46,XX (SRY positive) male syndrome].
    Shi D, Zhang Y, Zhou Y, Mao Q, Li H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Sep 10; 37(9):1039-1042. PubMed ID: 32820526
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  • 40. [Prenatal genetic diagnosis for a fetus with atypical neurofibromatosis type 1 microdeletion].
    Lin S, Wu J, Zhang Z, Ji Y, Fang Q, Chen B, Luo Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr 10; 33(2):212-5. PubMed ID: 27060318
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