These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

200 related items for PubMed ID: 29808250

  • 1. 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; 298(2):289-295. PubMed ID: 29808250
    [Abstract] [Full Text] [Related]

  • 2. 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; 225():19-21. PubMed ID: 29626710
    [Abstract] [Full Text] [Related]

  • 3. 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; 11(6):e2155. PubMed ID: 36849216
    [Abstract] [Full Text] [Related]

  • 4. [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]

  • 5. 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]

  • 6. 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]

  • 7. 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]

  • 8. [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]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Update on the clinical features and natural history of Wolf-Hirschhorn (4p-) syndrome: experience with 87 patients and recommendations for routine health supervision.
    Battaglia A, Filippi T, Carey JC.
    Am J Med Genet C Semin Med Genet; 2008 Nov 15; 148C(4):246-51. PubMed ID: 18932224
    [Abstract] [Full Text] [Related]

  • 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 15; 55(1):104-8. PubMed ID: 26927259
    [Abstract] [Full Text] [Related]

  • 12. On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review.
    Zollino M, Murdolo M, Marangi G, Pecile V, Galasso C, Mazzanti L, Neri G.
    Am J Med Genet C Semin Med Genet; 2008 Nov 15; 148C(4):257-69. PubMed ID: 18932124
    [Abstract] [Full Text] [Related]

  • 13. [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]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP, Jouannic JM, Bessières B, Borie C, Martin-Luis I, Fallet-Bianco C, Portnoï MF.
    Prenat Diagn; 2005 Jun 10; 25(6):451-5. PubMed ID: 15966060
    [Abstract] [Full Text] [Related]

  • 17. Risk of hepatic neoplasms in Wolf-Hirschhorn syndrome (4p-): Four new cases and review of the literature.
    Battaglia A, Calhoun ARUL, Lortz A, Carey JC.
    Am J Med Genet A; 2018 Nov 10; 176(11):2389-2394. PubMed ID: 30289612
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.