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3. 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]
4. Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the "critical segment" towards the telomere. Anvret M; Nordenskjöld M; Stolpe L; Johansson L; Bröndum-Nielsen K Hum Genet; 1991 Mar; 86(5):481-3. PubMed ID: 2016087 [TBL] [Abstract][Full Text] [Related]
5. Molecular and clinical characterization of a patient with a chromosome 4p deletion, Wolf-Hirschhorn syndrome, and congenital glaucoma. Finzi S; Pinto CF; Wiggs JL Ophthalmic Genet; 2001 Mar; 22(1):35-41. PubMed ID: 11262648 [TBL] [Abstract][Full Text] [Related]
6. Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)]. Wilson MG; Towner JW; Coffin GS; Ebbin AJ; Siris E; Brager P Hum Genet; 1981; 59(4):297-307. PubMed ID: 6949855 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Delimiting the Wolf-Hirschhorn syndrome critical region to 750 kilobase pairs. Altherr MR; Wright TJ; Denison K; Perez-Castro AV; Johnson VP Am J Med Genet; 1997 Jul; 71(1):47-53. PubMed ID: 9215768 [TBL] [Abstract][Full Text] [Related]
9. Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndrome. Quarrell OW; Snell RG; Curtis MA; Roberts SH; Harper PS; Shaw DJ J Med Genet; 1991 Apr; 28(4):256-9. PubMed ID: 1856831 [TBL] [Abstract][Full Text] [Related]
10. Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome. Zollino M; Di Stefano C; Zampino G; Mastroiacovo P; Wright TJ; Sorge G; Selicorni A; Tenconi R; Zappalà A; Battaglia A; Di Rocco M; Palka G; Pallotta R; Altherr MR; Neri G Am J Med Genet; 2000 Sep; 94(3):254-61. PubMed ID: 10995514 [TBL] [Abstract][Full Text] [Related]
11. Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3. Kant SG; Van Haeringen A; Bakker E; Stec I; Donnai D; Mollevanger P; Beverstock GC; Lindeman-Kusse MC; Van Ommen GJ J Med Genet; 1997 Jul; 34(7):569-72. PubMed ID: 9222965 [TBL] [Abstract][Full Text] [Related]
12. Interstitial deletion of the short arm of chromosome 4. Ray M; Evans J; Rockman-Greenberg C; Wickstrom D J Med Genet; 1984 Jun; 21(3):223-5. PubMed ID: 6748021 [TBL] [Abstract][Full Text] [Related]
13. A patient with Wolf-Hirschhorn syndrome originating from translocation t(4;8) (p16.3;q24.3)pat. el-Rifai W; Leisti J; Kähkönen M; Pietarinen A; Altherr MR; Knuutila S J Med Genet; 1995 Jan; 32(1):65-7. PubMed ID: 7897631 [TBL] [Abstract][Full Text] [Related]
14. Clinical, cytogenetic and molecular investigation in a fetus with Wolf-Hirschhorn syndrome with paternally derived 4p deletion. Case report and review of the literature. Dietze I; Fritz B; Huhle D; Simoens W; Piecha E; Rehder H Fetal Diagn Ther; 2004; 19(3):251-60. PubMed ID: 15067236 [TBL] [Abstract][Full Text] [Related]
15. A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf-Hirschhorn syndrome. Zollino M; Lecce R; Selicorni A; Murdolo M; Mancuso I; Marangi G; Zampino G; Garavelli L; Ferrarini A; Rocchi M; Opitz JM; Neri G Eur J Hum Genet; 2004 Oct; 12(10):797-804. PubMed ID: 15241479 [TBL] [Abstract][Full Text] [Related]
16. Molecular definition of the smallest region of deletion overlap in the Wolf-Hirschhorn syndrome. Gandelman KY; Gibson L; Meyn MS; Yang-Feng TL Am J Hum Genet; 1992 Sep; 51(3):571-8. PubMed ID: 1379774 [TBL] [Abstract][Full Text] [Related]
18. Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome. Tupler R; Bortotto L; Bühler EM; Alkan M; Malik NJ; Bösch-Al Jadooa N; Memo L; Maraschio P J Med Genet; 1992 Jan; 29(1):53-5. PubMed ID: 1552546 [TBL] [Abstract][Full Text] [Related]
19. Parental origin of chromosome 4p deletion in Wolf-Hirschhorn syndrome. Dallapiccola B; Mandich P; Bellone E; Selicorni A; Mokin V; Ajmar F; Novelli G Am J Med Genet; 1993 Nov; 47(6):921-4. PubMed ID: 7904122 [TBL] [Abstract][Full Text] [Related]
20. Familial interstitial deletion of the short arm of chromosome 4 (p15.33-p16.3) characterized by molecular cytogenetic analysis. Basinko A; Douet-Guilbert N; Parent P; Blondin G; Mingam M; Monot F; Morel F; Le Bris MJ; De Braekeleer M Am J Med Genet A; 2008 Apr; 146A(7):899-903. PubMed ID: 18302281 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]