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 *

190 related articles for article (PubMed ID: 31302910)

  • 1. [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; 36(7):682-685. PubMed ID: 31302910
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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; 34(5):714-717. PubMed ID: 28981940
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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; 32(4):512-4. PubMed ID: 26252097
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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; 41(10):1201-1205. PubMed ID: 39344614
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Prenatal diagnosis of a fetus with a cryptic translocation 4p;18p and Wolf-Hirschhorn syndrome (WHS).
    Kohlschmidt N; Zielinski J; Brude E; Schäfer D; Olert J; Hallermann C; Coerdt W; Arnemann J
    Prenat Diagn; 2000 Feb; 20(2):152-5. PubMed ID: 10694689
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [A case of Wolf-Hirschhorn syndrome diagnosed by single nucleotide polymorphism array].
    Jin Y; Liu X; Li S; Zhou C; Liu X; Song Q; Wang L; Miao Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Aug; 33(4):501-4. PubMed ID: 27455007
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4.
    Altherr MR; Bengtsson U; Elder FF; Ledbetter DH; Wasmuth JJ; McDonald ME; Gusella JF; Greenberg F
    Am J Hum Genet; 1991 Dec; 49(6):1235-42. PubMed ID: 1746553
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Microarray analysis of unbalanced translocation in Wolf-Hirschhorn syndrome.
    Dai Y; Yang J; Chen Y; Bao L; Cheng Q
    Pediatr Int; 2013 Jun; 55(3):368-70. PubMed ID: 23782367
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 4p16.3 microdeletions and microduplications detected by chromosomal microarray analysis: New insights into mechanisms and critical regions.
    Bi W; Cheung SW; Breman AM; Bacino CA
    Am J Med Genet A; 2016 Oct; 170(10):2540-50. PubMed ID: 27287194
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Trisomy 12p and monosomy 4p: phenotype-genotype correlation.
    Benussi DG; Costa P; Zollino M; Murdolo M; Petix V; Carrozzi M; Pecile V
    Genet Test Mol Biomarkers; 2009 Apr; 13(2):199-204. PubMed ID: 19378504
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 94(7):549-52. PubMed ID: 22641563
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 16(1):45-52. PubMed ID: 17726485
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Duplication of the Wolf-Hirschhorn syndrome critical region causes neurodevelopmental delay.
    Hannes F; Drozniewska M; Vermeesch JR; Haus O
    Eur J Med Genet; 2010; 53(3):136-40. PubMed ID: 20197130
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Diagnosis of familial Wolf-Hirschhorn syndrome due to a paternal cryptic chromosomal rearrangement by conventional and molecular cytogenetic techniques.
    Venegas-Vega CA; Fernández-Ramírez F; Zepeda LM; Nieto-Martínez K; Gómez-Laguna L; Garduño-Zarazúa LM; Berumen J; Kofman S; Cervantes A
    Biomed Res Int; 2013; 2013():209204. PubMed ID: 23484094
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Submicroscopic duplication of the Wolf-Hirschhorn critical region with a 4p terminal deletion.
    Roselló M; Monfort S; Orellana C; Ferrer-Bolufer I; Quiroga R; Oltra S; Martínez F
    Cytogenet Genome Res; 2009; 125(2):103-8. PubMed ID: 19729912
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16.
    Zollino M; Lecce R; Murdolo M; Orteschi D; Marangi G; Selicorni A; Midro A; Sorge G; Zampino G; Memo L; Battaglia D; Petersen M; Pandelia E; Gyftodimou Y; Faravelli F; Tenconi R; Garavelli L; Mazzanti L; Fischetto R; Cavalli P; Savasta S; Rodriguez L; Neri G
    Hum Genet; 2007 Dec; 122(5):423-30. PubMed ID: 17676343
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mild Wolf-Hirschhorn phenotype in a girl with unbalanced t(4p;12p) translocation without seizures.
    Galasso C; Lo-Castro A; El-Malhany N; Zollino M; Murdolo M; Orteschi D; Manca Bitti ML; Curatolo P
    Am J Med Genet A; 2010 Jan; 152A(1):258-61. PubMed ID: 20014124
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.