BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

188 related articles for article (PubMed ID: 18076104)

  • 1. Multiple hemangiomas in a patient with a t(3q;4p) translocation: an infrequent association with Wolf-Hirschhorn syndrome.
    Pardo S; Blitman N; Han B; Cohen N; Edelmann L; Hirschhorn K
    Am J Med Genet A; 2008 Jan; 146A(2):219-24. PubMed ID: 18076104
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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; 164A(3):597-609. PubMed ID: 24357569
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 4p16.1-p15.31 duplication and 4p terminal deletion in a 3-years old Chinese girl: Array-CGH, genotype-phenotype and neurological characterization.
    Piccione M; Salzano E; Vecchio D; Ferrara D; Malacarne M; Pierluigi M; Ferrara I; Corsello G
    Eur J Paediatr Neurol; 2015 Jul; 19(4):477-83. PubMed ID: 25769226
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotype.
    South ST; Whitby H; Maxwell T; Aston E; Brothman AR; Carey JC
    Am J Med Genet A; 2008 Oct; 146A(20):2691-7. PubMed ID: 18798325
    [TBL] [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; 148C(4):246-51. PubMed ID: 18932224
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pediatric diagnosis not made until adulthood: a case of Wolf-Hirschhorn syndrome.
    Coppola A; Chinthapalli K; Hammond P; Sander JW; Sisodiya SM
    Gene; 2013 Jan; 512(2):532-5. PubMed ID: 23064045
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Wolf-Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter.
    Iwanowski PS; Panasiuk B; Van Buggenhout G; Murdolo M; Myśliwiec M; Maas NM; Lattante S; Korniszewski L; Posmyk R; Pilch J; Zajączek S; Fryns JP; Zollino M; Midro AT
    Am J Med Genet A; 2011 Aug; 155A(8):1833-47. PubMed ID: 21744486
    [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. 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]  

  • 15. Pathogenic significance of deletions distal to the currently described Wolf-Hirschhorn syndrome critical regions on 4p16.3.
    South ST; Hannes F; Fisch GS; Vermeesch JR; Zollino M
    Am J Med Genet C Semin Med Genet; 2008 Nov; 148C(4):270-4. PubMed ID: 18932125
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 148C(4):257-69. PubMed ID: 18932124
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Wolf-Hirschhorn Syndrome with Epibulbar Dermoid: An Unusual Association in a Patient with 4p Deletion and Functional Xp Disomy.
    Bragagnolo S; Colovati ME; Guilherme RS; Dantas AG; de Souza MZ; de Soares MF; Melaragno MI; Perez AB
    Cytogenet Genome Res; 2016; 150(1):17-22. PubMed ID: 27842301
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical characterization and proposed mechanism of juvenile glaucoma--a patient with a chromosome 4p deletion, Wolf-Hirschhorn Syndrome.
    Curtin J; Moloney G; Grigg J; Sharota Franzco D
    Ophthalmic Genet; 2010 Sep; 31(3):135-8. PubMed ID: 20569021
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical features in adult patient with Wolf-Hirschhorn syndrome.
    Martínez-Quintana E; Rodríguez-González F
    Morphologie; 2014 Jun; 98(321):86-9. PubMed ID: 24656633
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.