305 related articles for article (PubMed ID: 18932125)
1. 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]
2. 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]
3. 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]
4. Wolf Hirshhorn syndrome in a case of ring chromosome 4: phenotype and molecular cytogenetic findings.
Laleye A; Alao MJ; Adjagba M; Hans C; Delneste D; Gnamey DK; Ayivi B; Darboux RB
Genet Couns; 2006; 17(1):35-40. PubMed ID: 16719275
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. "Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype.
Zollino M; Wright TJ; Di Stefano C; Tosolini A; Battaglia A; Altherr MR; Neri G
Am J Med Genet; 1999 Feb; 82(5):371-5. PubMed ID: 10069706
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Mouse models of Wolf-Hirschhorn syndrome.
Simon R; Bergemann AD
Am J Med Genet C Semin Med Genet; 2008 Nov; 148C(4):275-80. PubMed ID: 18932126
[TBL] [Abstract][Full Text] [Related]
16. Distal 4p microdeletion in a case of Wolf-Hirschhorn syndrome with congenital diaphragmatic hernia.
Casaccia G; Mobili L; Braguglia A; Santoro F; Bagolan P
Birth Defects Res A Clin Mol Teratol; 2006 Mar; 76(3):210-3. PubMed ID: 16498629
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. FISH detection of Wolf-Hirschhorn syndrome: exclusion of D4F26 as critical site.
Johnson VP; Altherr MR; Blake JM; Keppen LD
Am J Med Genet; 1994 Aug; 52(1):70-4. PubMed ID: 7977466
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1-->pter) and partial trisomy 10q (10q25.1-->qter).
Chen CP; Chen YJ; Chern SR; Tsai FJ; Chang TY; Lee CC; Town DD; Lee MS; Wang W
Prenat Diagn; 2008 May; 28(5):450-3. PubMed ID: 18395879
[No Abstract] [Full Text] [Related]
[Next] [New Search]
