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 *

174 related articles for article (PubMed ID: 25741211)

  • 21. High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome.
    Fang YY; Bain S; Haan EA; Eyre HJ; MacDonald M; Wright TJ; Altherr MR; Riess O; Sutherland G; Callen DF
    Am J Med Genet; 1997 Sep; 71(4):453-7. PubMed ID: 9286454
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Diagnosis of a terminal deletion of 4p with duplication of Xp22.31 in a patient with findings of Opitz G/BBB syndrome and Wolf-Hirschhorn syndrome.
    So J; Müller I; Kunath M; Herrmann S; Ullmann R; Schweiger S
    Am J Med Genet A; 2008 Jan; 146A(1):103-9. PubMed ID: 18074389
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder.
    Zollino M; Orteschi D; Ruiter M; Pfundt R; Steindl K; Cafiero C; Ricciardi S; Contaldo I; Chieffo D; Ranalli D; Acquafondata C; Murdolo M; Marangi G; Asaro A; Battaglia D
    Epilepsia; 2014 Jun; 55(6):849-57. PubMed ID: 24738919
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The delineation of the Wolf-Hirschhorn syndrome over six decades: Illustration of the ongoing advances in phenotype analysis and cytogenomic technology.
    Battaglia A; Carey JC
    Am J Med Genet A; 2021 Sep; 185(9):2748-2755. PubMed ID: 34002939
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Microarray-based comparative genomic hybridization analysis of Wolf-Hirschhorn syndrome in a fetus with deletion of 4p15.3 to 4pter.
    Chao A; Lee YS; Chao AS; Wang TH; Chang SD
    Birth Defects Res A Clin Mol Teratol; 2006 Oct; 76(10):739-43. PubMed ID: 17022067
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Interstitial deletion of distal chromosome 4p in a patient without classical Wolf-Hirschhorn syndrome.
    Estabrooks LL; Rao KW; Korf B
    Am J Med Genet; 1993 Jan; 45(1):97-100. PubMed ID: 8418669
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Unmasking of a hemizygous WFS1 gene mutation by a chromosome 4p deletion of 8.3 Mb in a patient with Wolf-Hirschhorn syndrome.
    Flipsen-ten Berg K; van Hasselt PM; Eleveld MJ; van der Wijst SE; Hol FA; de Vroede MA; Beemer FA; Hochstenbach PF; Poot M
    Eur J Hum Genet; 2007 Nov; 15(11):1132-8. PubMed ID: 17637805
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Analyses of Genotypes and Phenotypes of Ten Chinese Patients with Wolf-Hirschhorn Syndrome by Multiplex Ligation-dependent Probe Amplification and Array Comparative Genomic Hybridization.
    Yang WX; Pan H; Li L; Wu HR; Wang ST; Bao XH; Jiang YW; Qi Y
    Chin Med J (Engl); 2016 Mar; 129(6):672-8. PubMed ID: 26960370
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Natural histories of patients with Wolf-Hirschhorn syndrome derived from variable chromosomal abnormalities.
    Yamamoto-Shimojima K; Kouwaki M; Kawashima Y; Itomi K; Momosaki K; Ozasa S; Okamoto N; Yokochi K; Yamamoto T
    Congenit Anom (Kyoto); 2019 Sep; 59(5):169-173. PubMed ID: 30378700
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genotype-phenotype correlation in 21 patients with Wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH).
    Maas NM; Van Buggenhout G; Hannes F; Thienpont B; Sanlaville D; Kok K; Midro A; Andrieux J; Anderlid BM; Schoumans J; Hordijk R; Devriendt K; Fryns JP; Vermeesch JR
    J Med Genet; 2008 Feb; 45(2):71-80. PubMed ID: 17873117
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mapping the Wolf-Hirschhorn syndrome phenotype outside the currently accepted WHS critical region and defining a new critical region, WHSCR-2.
    Zollino M; Lecce R; Fischetto R; Murdolo M; Faravelli F; Selicorni A; Buttè C; Memo L; Capovilla G; Neri G
    Am J Hum Genet; 2003 Mar; 72(3):590-7. PubMed ID: 12563561
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Molecular and clinical characterization of a patient with a chromosome 4p deletion, Wolf-Hirschhorn syndrome, and congenital glaucoma.
    Finzi S; Pinto CF; Wiggs JL
    Ophthalmic Genet; 2001 Mar; 22(1):35-41. PubMed ID: 11262648
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Malignant hematological disorders in children with Wolf-Hirschhorn syndrome.
    Sharathkumar A; Kirby M; Freedman M; Abdelhaleem M; Chitayat D; Teshima IE; Dror Y
    Am J Med Genet A; 2003 Jun; 119A(2):194-9. PubMed ID: 12749063
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. A large Indian family with rearrangement of chromosome 4p16 and 3p26.3 and divergent clinical presentations.
    Iype T; Alakbarzade V; Iype M; Singh R; Sreekantan-Nair A; Chioza BA; Mohapatra TM; Baple EL; Patton MA; Warner TT; Proukakis C; Kulkarni A; Crosby AH
    BMC Med Genet; 2015 Nov; 16():104. PubMed ID: 26554554
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. 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; 97(12):806-11. PubMed ID: 24343879
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Wolf-Hirschhorn Syndrome: Clinical and Genetic Data from a First Case Diagnosed in Central Africa.
    Mbuyi-Musanzayi S; Lumaka A; Kasole TL; Ilunga EK; Asani BY; Tshilobo PL; Muenze PK; Reychler H; Katombe FT; Devriendt K
    J Pediatr Genet; 2017 Sep; 6(3):186-190. PubMed ID: 28794913
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.