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

606 related items for PubMed ID: 26927259

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

  • 2. 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; 50(4):506-11. PubMed ID: 22212326
    [Abstract] [Full Text] [Related]

  • 3. 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; 56(6):821-826. PubMed ID: 29241927
    [Abstract] [Full Text] [Related]

  • 4. 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; 59(3):425-431. PubMed ID: 32416892
    [Abstract] [Full Text] [Related]

  • 5. [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; 50(6):460-4. PubMed ID: 22931946
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. [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]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. 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]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family.
    Chen CP, Chang SD, Wang TH, Wang LK, Tsai JD, Liu YP, Chern SR, Wu PS, Su JW, Chen YT, Wang W.
    Taiwan J Obstet Gynecol; 2013 Dec 10; 52(4):551-7. PubMed ID: 24411042
    [Abstract] [Full Text] [Related]

  • 19. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.
    Chen CP, Chen M, Ko TM, Ma GC, Tsai FJ, Tsai MS, Wu PC, Lee CC, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2010 Dec 10; 49(4):500-5. PubMed ID: 21199754
    [Abstract] [Full Text] [Related]

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

    Page: [Next] [New Search]
    of 31.