170 related articles for article (PubMed ID: 17941887)
1. Interstitial deletion of chromosome 4p associated with mild mental retardation, epilepsy and polymicrogyria of the left temporal lobe.
Møller RS; Hansen CP; Jackson GD; Ullmann R; Ropers HH; Tommerup N; Tümer Z
Clin Genet; 2007 Dec; 72(6):593-8. PubMed ID: 17941887
[TBL] [Abstract][Full Text] [Related]
2. Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardation.
White DM; Pillers DA; Reiss JA; Brown MG; Magenis RE
Am J Med Genet; 1995 Jul; 57(4):588-97. PubMed ID: 7573135
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literature.
Chitayat D; Ruvalcaba RH; Babul R; Teshima IE; Posnick JC; Vekemans MJ; Scarpelli H; Thuline H
Am J Med Genet; 1995 Jan; 55(2):147-54. PubMed ID: 7717413
[TBL] [Abstract][Full Text] [Related]
5. Periventricular heterotopia in a boy with interstitial deletion of chromosome 4p.
Gawlik-Kuklinska K; Wierzba J; Wozniak A; Iliszko M; Debiec-Rychter M; Dubaniewicz-Wybieralska M; Limon J
Eur J Med Genet; 2008; 51(2):165-71. PubMed ID: 18243084
[TBL] [Abstract][Full Text] [Related]
6. [Epilepsy in three children with Wolf-Hirschhorn syndrome].
Kaciński M; Kostyk E; Kruczek A; Skowronek-Bała B
Przegl Lek; 2005; 62(11):1298-301. PubMed ID: 16512625
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Mild phenotype in interstitial 4p deletion: another patient and review of the literature.
Van de Graaf G; Sijstermans JM; Engelen JJ; Schrander-Stumpel CT
Genet Couns; 1997; 8(1):13-8. PubMed ID: 9101273
[TBL] [Abstract][Full Text] [Related]
9. Interstitial deletion of 4p15.32p16.3 in a boy with minor anomalies, hearing loss, borderline intelligence, and oligodontia.
Kozma C; Chong SS; Meck JM
Am J Med Genet; 1999 Oct; 86(4):316-20. PubMed ID: 10494085
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Bilateral polymicrogyria as the indicative feature in a child with a 22q11.2 deletion.
Gerkes EH; Hordijk R; Dijkhuizen T; Sival DA; Meiners LC; Sikkema-Raddatz B; van Ravenswaaij-Arts CM
Eur J Med Genet; 2010; 53(5):344-6. PubMed ID: 20553986
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis and molecular cytogenetic characterization of a de novo proximal interstitial deletion of chromosome 4p (4p15.2→p14).
Chen CP; Lee MJ; Chern SR; Wu PS; Su JW; Chen YT; Lee MS; Wang W
Gene; 2013 Oct; 529(2):351-6. PubMed ID: 23948085
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. A case of Wolf-Hirschhorn syndrome progressing to resistant epilepsy.
Unalp A; Uran N; Giray O; Ercal D
Pediatr Neurol; 2007 Aug; 37(2):140-3. PubMed ID: 17675032
[TBL] [Abstract][Full Text] [Related]
16. Deletion of chromosome 21 in a girl with congenital hypothyroidism and mild mental retardation.
Ahlbom BE; Sidenvall R; Annerén G
Am J Med Genet; 1996 Aug; 64(3):501-5. PubMed ID: 8862630
[TBL] [Abstract][Full Text] [Related]
17. 6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.
Elia M; Striano P; Fichera M; Gaggero R; Castiglia L; Galesi O; Malacarne M; Pierluigi M; Amato C; Musumeci SA; Romano C; Majore S; Grammatico P; Zara F; Striano S; Faravelli F
Epilepsia; 2006 May; 47(5):830-8. PubMed ID: 16686647
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. De novo interstitial deletion of 9q32-34.1 with mental retardation, developmental delay, epilepsy, and cortical dysplasia: a case report.
Tos T; Alp MY; Karacan CD; Andiran N; Colakoglu EY
Genet Couns; 2014; 25(2):197-201. PubMed ID: 25059019
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
