267 related articles for article (PubMed ID: 27842301)
1. 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]
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. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. [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]
9. 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]
10. 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]
11. Wolf-Hirschhorn syndrome: A case series from India.
Chaudhry C; Kaur A; Panigrahi I; Kaur A
Am J Med Genet A; 2020 Dec; 182(12):3048-3051. PubMed ID: 32914558
[TBL] [Abstract][Full Text] [Related]
12. Congenital cavitary optic disc anomaly and Axenfeld's anomaly in Wolf-Hirschhorn syndrome: A case report and review of the literature.
Ali MH; Azar NF; Aakalu V; Chau FY; Abbasian J; Setabutr P; Maumenee IH
Ophthalmic Genet; 2018 Apr; 39(2):271-274. PubMed ID: 29199884
[TBL] [Abstract][Full Text] [Related]
13. Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf-Hirschhorn syndrome.
Ho KS; South ST; Lortz A; Hensel CH; Sdano MR; Vanzo RJ; Martin MM; Peiffer A; Lambert CG; Calhoun A; Carey JC; Battaglia A
J Med Genet; 2016 Apr; 53(4):256-63. PubMed ID: 26747863
[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. 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]
16. 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]
17. Microduplication of 4p16.3 due to an unbalanced translocation resulting in a mild phenotype.
Carmany EP; Bawle EV
Am J Med Genet A; 2011 Apr; 155A(4):819-24. PubMed ID: 21412978
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. 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]
20. Hepatic Malignancy in an Infant with Wolf-Hirschhorn Syndrome.
Rutter S; Morotti RA; Peterec S; Gallagher PG
Fetal Pediatr Pathol; 2017 Jun; 36(3):256-262. PubMed ID: 28266898
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
