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Journal Abstract Search

194 related items for PubMed ID: 27455007

  • 1.
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  • 2. [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
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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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  • 5. [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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  • 6. Wolf-Hirschhorn syndrome: a case with normal karyotype, demonstrated by array CGH (aCGH).
    Saberi A, Shariati G, Hamid M, Galehdari H, Abdorasouli N.
    Arch Iran Med; 2014 Sep 10; 17(9):642-4. PubMed ID: 25204484
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  • 8. [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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  • 9. Three patients with Wolf-Hirschhorn syndrome carrying a satellited chromosome 4p.
    Liang D, Zhou Z, Meng D, Du J, Wen J, Niikawa N, Wu L.
    Birth Defects Res A Clin Mol Teratol; 2012 Jul 10; 94(7):549-52. PubMed ID: 22641563
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  • 10. 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
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  • 12. Microarray and FISH-based genotype-phenotype analysis of 22 Japanese patients with Wolf-Hirschhorn syndrome.
    Shimizu K, Wakui K, Kosho T, Okamoto N, Mizuno S, Itomi K, Hattori S, Nishio K, Samura O, Kobayashi Y, Kako Y, Arai T, Tsutomu OI, Kawame H, Narumi Y, Ohashi H, Fukushima Y.
    Am J Med Genet A; 2014 Mar 10; 164A(3):597-609. PubMed ID: 24357569
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  • 13. Inv dup del(4)(:p14 --> p16.3::p16.3 --> qter) with manifestations of partial duplication 4p and Wolf-Hirschhorn syndrome.
    Kondoh Y, Toma T, Ohashi H, Harada N, Yoshiura K, Ohta T, Kishino T, Niikawa N, Matsumoto N.
    Am J Med Genet A; 2003 Jul 01; 120A(1):123-6. PubMed ID: 12794704
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  • 14. Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.
    Chen CP, Su YN, Chen YY, Su JW, Chern SR, Chen YT, Chen WL, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2011 Dec 01; 50(4):506-11. PubMed ID: 22212326
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  • 15. Microarray analysis of unbalanced translocation in Wolf-Hirschhorn syndrome.
    Dai Y, Yang J, Chen Y, Bao L, Cheng Q.
    Pediatr Int; 2013 Jun 01; 55(3):368-70. PubMed ID: 23782367
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  • 16. Comprehensive analysis of Wolf-Hirschhorn syndrome using array CGH indicates a high prevalence of translocations.
    South ST, Whitby H, Battaglia A, Carey JC, Brothman AR.
    Eur J Hum Genet; 2008 Jan 01; 16(1):45-52. PubMed ID: 17726485
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  • 17. Clinical and genetic characterization of ten Egyptian patients with Wolf-Hirschhorn syndrome and review of literature.
    Mekkawy MK, Kamel AK, Thomas MM, Ashaat EA, Zaki MS, Eid OM, Ismail S, Hammad SA, Megahed H, ElAwady H, Refaat KM, Hussien S, Helmy N, Abd Allah SG, Mohamed AM, El Ruby MO.
    Mol Genet Genomic Med; 2021 Feb 01; 9(2):e1546. PubMed ID: 33217222
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  • 18. [Genetic analysis of a child with XYY syndrome mainly featuring mental retardation].
    Liu Y, Dong R, Zhang K, Wang Y, Zhang H, Zhang Y, Zhao D, Gai Z.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct 01; 33(5):686-9. PubMed ID: 27577224
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  • 19. Wolf-Hirschhorn Syndrome with Epibulbar Dermoid: An Unusual Association in a Patient with 4p Deletion and Functional Xp Disomy.
    Bragagnolo S, Colovati ME, Guilherme RS, Dantas AG, de Souza MZ, de Soares MF, Melaragno MI, Perez AB.
    Cytogenet Genome Res; 2016 Oct 01; 150(1):17-22. PubMed ID: 27842301
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  • 20. [Diagnosis of a case with Williams-Beuren syndrome by single nucleotide polymorphism array].
    Jin Y, Liu X, Li S, Ge J, Wu X, Song Q, Zhou C, Miao Z.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Aug 01; 32(4):529-32. PubMed ID: 26252101
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