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149 related items for PubMed ID: 34365613

  • 1. [Study on clinical features and diagnostic methods of prenatal Wolf-Hirschhorn syndrome].
    Wang Y, Chen X, Xue H, Chen L, Chen M, Huang H, He D, Xu L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Aug 10; 38(8):735-739. PubMed ID: 34365613
    [Abstract] [Full Text] [Related]

  • 2. [Prenatal diagnosis and genetic analysis of two fetuses with Wolf-Hirschhorn syndrome].
    Li F, Wu A, Xie X, Ma M, Tang J, Tang S, Tan W, Yin W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Oct 10; 41(10):1201-1205. PubMed ID: 39344614
    [Abstract] [Full Text] [Related]

  • 3. [Identification of a critical region on chromosome 4p16.3 for Wolf-Hirschhorn syndrome-associated fetal growth retardation].
    Zheng W, Chen B, Yin Z, Huang X, Liang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jul 10; 37(7):731-735. PubMed ID: 32619252
    [Abstract] [Full Text] [Related]

  • 4. Prenatal Diagnosis and Molecular Cytogenetic Analyses of a de novo Deletion on Chromosome 4p16.3p15.33.
    Luo H, Chang R, Liu F, Gao X.
    Altern Ther Health Med; 2023 Nov 10; 29(8):907-909. PubMed ID: 37708564
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Prenatal phenotype of Wolf-Hirschhorn syndrome: A case series and literature review.
    Tang F, Zeng Y, Wang L, Yin D, Chen L, Xie D, Wang J.
    Mol Genet Genomic Med; 2023 Jun 10; 11(6):e2155. PubMed ID: 36849216
    [Abstract] [Full Text] [Related]

  • 7. Prenatal diagnosis of Wolf-Hirschhorn syndrome: Ultrasonography and molecular karyotyping results.
    Zhen L, Fan SS, Huang LY, Pan M, Han J, Yang X, Li DZ.
    Eur J Obstet Gynecol Reprod Biol; 2018 Jun 10; 225():19-21. PubMed ID: 29626710
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. 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 10; 50(4):506-11. PubMed ID: 22212326
    [Abstract] [Full Text] [Related]

  • 10. Prenatal ultrasound findings observed in the Wolf-Hirschhorn syndrome: data from the registry of congenital malformations in Auvergne.
    Debost-Legrand A, Goumy C, Laurichesse-Delmas H, Déchelotte P, Beaufrère AM, Lémery D, Francannet C, Gallot D.
    Birth Defects Res A Clin Mol Teratol; 2013 Dec 10; 97(12):806-11. PubMed ID: 24343879
    [Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones.
    Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2017 Dec 10; 56(6):821-826. PubMed ID: 29241927
    [Abstract] [Full Text] [Related]

  • 12. [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]

  • 13. Wolf-Hirschhorn syndrome: Prenatal diagnosis and molecular cytogenetic characterization of a de novo distal deletion of 4p (4p16.1 → pter) in a fetus with facial cleft and preaxial polydactyly.
    Chen CP, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Chen YY, Wang W.
    Taiwan J Obstet Gynecol; 2020 May 10; 59(3):425-431. PubMed ID: 32416892
    [Abstract] [Full Text] [Related]

  • 14. Cytogenomic Integrative Network Analysis of the Critical Region Associated with Wolf-Hirschhorn Syndrome.
    Corrêa T, Mergener R, Leite JCL, Galera MF, Moreira LMA, Vargas JE, Riegel M.
    Biomed Res Int; 2018 May 10; 2018():5436187. PubMed ID: 29721507
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  • 18. Wolf-Hirschhorn syndrome: A case series from India.
    Chaudhry C, Kaur A, Panigrahi I, Kaur A.
    Am J Med Genet A; 2020 Dec 10; 182(12):3048-3051. PubMed ID: 32914558
    [Abstract] [Full Text] [Related]

  • 19. Prenatal sonographic findings in confirmed cases of Wolf-Hirschhorn syndrome.
    Simonini C, Hoopmann M, Kagan KO, Schröder T, Gembruch U, Geipel A.
    BMC Pregnancy Childbirth; 2022 Apr 15; 22(1):327. PubMed ID: 35428251
    [Abstract] [Full Text] [Related]

  • 20. 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 15; 17(9):642-4. PubMed ID: 25204484
    [Abstract] [Full Text] [Related]

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