921 related articles for article (PubMed ID: 18932124)
1. 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]
2. 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]
3. 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]
4. 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]
5. Preliminary phenotypic map of chromosome 4p16 based on 4p deletions.
Estabrooks LL; Rao KW; Driscoll DA; Crandall BF; Dean JC; Ikonen E; Korf B; Aylsworth AS
Am J Med Genet; 1995 Jul; 57(4):581-6. PubMed ID: 7573133
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. "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]
8. 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]
9. 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]
10. 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]
11. 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]
12. Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletion.
Wieczorek D; Krause M; Majewski F; Albrecht B; Horn D; Riess O; Gillessen-Kaesbach G
Eur J Hum Genet; 2000 Jul; 8(7):519-26. PubMed ID: 10909852
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. 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]
17. 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]
18. 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]
19. Wolf-Hirschhorn (4P-) syndrome in adults.
Marcelis C; Schrander-Stumpel C; Engelen J; Schoonbrood-Lenssen A; Willemse A; Beemer F; Sigaudy S; Missirian C; Philip N; Fryns JP
Genet Couns; 2001; 12(1):35-48. PubMed ID: 11332977
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
