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2. Management of sleeping problems in Wolf-Hirschhorn syndrome: a case study. Curfs LM; Didden R; Sikkema SP; De Die-Smulders CE Genet Couns; 1999; 10(4):345-50. PubMed ID: 10631921 [TBL] [Abstract][Full Text] [Related]
3. [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]
4. The Wolf-Hirschhorn syndrome. New endocrine data. Ioan D; Hîrşovescu N; Dumitriu L; Goldstein R; Cernea LC; Bareliuc L; Mîrşeanu M; Maximilian C Endocrinologie; 1985; 23(1):67-72. PubMed ID: 3992159 [TBL] [Abstract][Full Text] [Related]
5. Seizure and EEG patterns in Wolf-Hirschhorn (4p-) syndrome. Battaglia A; Carey JC Brain Dev; 2005 Aug; 27(5):362-4. PubMed ID: 16023553 [TBL] [Abstract][Full Text] [Related]
6. Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter). Syrrou M; Borghgraef M; Fryns JP Am J Med Genet; 2001 Dec; 104(3):199-203. PubMed ID: 11754044 [TBL] [Abstract][Full Text] [Related]
7. A mosaic extra ring chromosome 4 in a female patient with postnatal overgrowth. Vermeesch JR; Petit P; Dutra A; Schröck E; Ried T; Fryns JP Genet Couns; 1999; 10(2):195-6. PubMed ID: 10422016 [No 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. Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype map. Van Buggenhout G; Melotte C; Dutta B; Froyen G; Van Hummelen P; Marynen P; Matthijs G; de Ravel T; Devriendt K; Fryns JP; Vermeesch JR J Med Genet; 2004 Sep; 41(9):691-8. PubMed ID: 15342700 [No Abstract] [Full Text] [Related]
12. 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]
13. Wolf-Hirschhorn syndrome and the 4p-related syndromes. Battaglia A; Carey JC Am J Med Genet C Semin Med Genet; 2008 Nov; 148C(4):241-3. PubMed ID: 18932222 [No Abstract] [Full Text] [Related]
15. Prenatal diagnosis of brain abnormalities in Wolf-Hirschhorn (4p-) syndrome. De Keersmaecker B; Albert M; Hillion Y; Ville Y Prenat Diagn; 2002 May; 22(5):366-70. PubMed ID: 12001188 [TBL] [Abstract][Full Text] [Related]
16. 4p terminal deletion and 11p subtelomeric duplication detected by genomic microarray in a patient with Wolf-Hirschhorn syndrome and an atypical phenotype. Stevenson DA; Carey JC; Cowley BC; Bayrak-Toydemir P; Mao R; Brothman AR J Pediatr; 2004 Dec; 145(6):840-2. PubMed ID: 15580214 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Health supervision and anticipatory guidance of individuals with Wolf-Hirschhorn syndrome. Battaglia A; Carey JC Am J Med Genet; 1999 Jun; 89(2):111-5. PubMed ID: 10559766 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. The human homeobox gene HOX7 maps to chromosome 4p16.1 and may be implicated in Wolf-Hirschhorn syndrome. Ivens A; Flavin N; Williamson R; Dixon M; Bates G; Buckingham M; Robert B Hum Genet; 1990 Apr; 84(5):473-6. PubMed ID: 1969845 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]