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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 24455347)

  • 1. Prenatal diagnosis of 4p and 4q subtelomeric microdeletion in de novo ring chromosome 4.
    Akbas H; Cine N; Erdemoglu M; Atay AE; Simsek S; Turkyilmaz A; Fidanboy M
    Case Rep Obstet Gynecol; 2013; 2013():248050. PubMed ID: 24455347
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [A case of mosaic ring chromosome 4 with subtelomeric 4p deletion].
    Kim JH; Oh PS; Na HY; Kim SH; Cho HC
    Korean J Lab Med; 2009 Feb; 29(1):77-81. PubMed ID: 19262083
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 25(6):451-5. PubMed ID: 15966060
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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; 37(7):731-735. PubMed ID: 32619252
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal Diagnosis of 4q Terminal Deletion and Review of the Literature.
    Tidrenczel Z; Tardy EP; Pikó H; Sarkadi E; Böjtös I; Demeter J; Simon J; Kósa JP; Beke A
    Cytogenet Genome Res; 2019; 158(2):63-73. PubMed ID: 31261151
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Complex de novo cryptic subtelomeric rearrangements in a fetus with multiple ultrasonographic abnormalities and a normal karyotype at amniocentesis.
    Iqbal MA; Ramadan S; Ali FA; Kurdi W
    Prenat Diagn; 2005 Dec; 25(12):1142-9. PubMed ID: 16240463
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of de novo unbalanced translocation 8p;21q using subtelomeric probes.
    Ozkinay F; Kanit H; Onay H; Cogulu O; Gunduz C; Ercal D; Ozkinay C
    Genet Couns; 2006; 17(3):315-20. PubMed ID: 17100200
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 15q24 microdeletion.
    Chen CP; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2020 May; 59(3):432-436. PubMed ID: 32416893
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical, cytogenetic and molecular investigation in a fetus with Wolf-Hirschhorn syndrome with paternally derived 4p deletion. Case report and review of the literature.
    Dietze I; Fritz B; Huhle D; Simoens W; Piecha E; Rehder H
    Fetal Diagn Ther; 2004; 19(3):251-60. PubMed ID: 15067236
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and molecular description of a fetus in prenatal diagnosis with a rare de novo ring 10 and deletions of 12.59 Mb in 10p15.3-p14 and 4.22 Mb in 10q26.3.
    Christopoulou G; Tzetis M; Konstantinidou AE; Tsezou A; Kanavakis E; Kitsiou-Tzeli S; Velissariou V
    Eur J Med Genet; 2012 Jan; 55(1):75-9. PubMed ID: 21914491
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal Diagnosis of Combined Maternal 4q Interstitial Deletion and Paternal 15q Microduplication.
    Libotte F; Fabiani M; Margiotti K; Viola A; Mesoraca A; Giorlandino C
    Genes (Basel); 2021 Oct; 12(10):. PubMed ID: 34681020
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
    Chen CP; Huang HK; Ling PY; Su YN; Chen M; Tsai FJ; Wu PC; Chern SR; Chen YT; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2011 Dec; 50(4):492-8. PubMed ID: 22212323
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis and molecular cytogenetic characterization of a de novo proximal interstitial deletion of chromosome 4p (4p15.2→p14).
    Chen CP; Lee MJ; Chern SR; Wu PS; Su JW; Chen YT; Lee MS; Wang W
    Gene; 2013 Oct; 529(2):351-6. PubMed ID: 23948085
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of a de novo ring chromosome 11.
    Mohamed AN; Ebrahim SA; Aatre R; Qureshi F; Jacques SM; Evans MI
    Am J Med Genet; 2001 Sep; 102(4):368-71. PubMed ID: 11503165
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Deletion of a 760 kb region at 4p16 determines the prenatal and postnatal growth retardation characteristic of Wolf-Hirschhorn syndrome.
    Concolino D; Rossi E; Strisciuglio P; Iembo MA; Giorda R; Ciccone R; Tenconi R; Zuffardi O
    J Med Genet; 2007 Oct; 44(10):647-50. PubMed ID: 17911656
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of de novo terminal deletion of chromosome 7q.
    Chen CP; Chern SR; Chang TY; Tzen CY; Lee CC; Chen WL; Lee MS; Wang W
    Prenat Diagn; 2003 May; 23(5):375-9. PubMed ID: 12749033
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.