These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
285 related articles for article (PubMed ID: 26275939)
1. Molecular and clinical characterization of Waardenburg syndrome type I in an Iranian cohort with two novel PAX3 mutations. Jalilian N; Tabatabaiefar MA; Farhadi M; Bahrami T; Emamdjomeh H; Noori-Daloii MR Gene; 2015 Dec; 574(2):302-7. PubMed ID: 26275939 [TBL] [Abstract][Full Text] [Related]
2. A novel mutation in the PAX3 gene causes Waardenburg syndrome type I in an Iranian family. Jalilian N; Tabatabaiefar MA; Farhadi M; Bahrami T; Noori-Daloii MR Int J Pediatr Otorhinolaryngol; 2015 Oct; 79(10):1736-40. PubMed ID: 26279250 [TBL] [Abstract][Full Text] [Related]
3. Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report. Zardadi S; Rayat S; Doabsari MH; Alishiri A; Keramatipour M; Shahri ZJ; Morovvati S BMC Pediatr; 2021 Feb; 21(1):70. PubMed ID: 33557787 [TBL] [Abstract][Full Text] [Related]
4. The value of MLPA in Waardenburg syndrome. Milunsky JM; Maher TA; Ito M; Milunsky A Genet Test; 2007; 11(2):179-82. PubMed ID: 17627390 [TBL] [Abstract][Full Text] [Related]
5. Novel PAX3 mutations causing Waardenburg syndrome type 1 in Tunisian patients. Trabelsi M; Nouira M; Maazoul F; Kraoua L; Meddeb R; Ouertani I; Chelly I; Benoit V; Besbes G; Mrad R Int J Pediatr Otorhinolaryngol; 2017 Dec; 103():14-19. PubMed ID: 29224756 [TBL] [Abstract][Full Text] [Related]
6. Nonsense mutations in the PAX3 gene cause Waardenburg syndrome type I in two Chinese patients. Yang SZ; Cao JY; Zhang RN; Liu LX; Liu X; Zhang X; Kang DY; Li M; Han DY; Yuan HJ; Yang WY Chin Med J (Engl); 2007 Jan; 120(1):46-9. PubMed ID: 17254487 [TBL] [Abstract][Full Text] [Related]
7. SOX10 mutation causes Waardenburg syndrome associated with distinctive phenotypic features in an Iranian family: A clue for phenotype-directed genetic analysis. Jalilian N; Tabatabaiefar MA; Alimadadi H; Noori-Daloii MR Int J Pediatr Otorhinolaryngol; 2017 May; 96():122-126. PubMed ID: 28390600 [TBL] [Abstract][Full Text] [Related]
8. Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I. Niu Z; Li J; Tang F; Sun J; Wang X; Jiang L; Mei L; Chen H; Liu Y; Cai X; Feng Y; He C Gene; 2018 Feb; 642():362-366. PubMed ID: 29158168 [TBL] [Abstract][Full Text] [Related]
9. Identification of a novel mutation in the paired domain of PAX3 in an Iranian family with waardenburg syndrome type I. Sotirova VN; Rezaie TM; Khoshsorour MM; Sarfarazi M Ophthalmic Genet; 2000 Mar; 21(1):25-8. PubMed ID: 10779847 [TBL] [Abstract][Full Text] [Related]
10. The clinical and genetic research of Waardenburg syndrome type I and II in Chinese families. Liu Q; Cheng J; Lu Y; Zhou J; Wang L; Yang C; Yang G; Yang H; Cao J; Zhang Z; Sun Y Int J Pediatr Otorhinolaryngol; 2020 Mar; 130():109806. PubMed ID: 31812001 [TBL] [Abstract][Full Text] [Related]
11. Genetic analysis of PAX3 for diagnosis of Waardenburg syndrome type I. Matsunaga T; Mutai H; Namba K; Morita N; Masuda S Acta Otolaryngol; 2013 Apr; 133(4):345-51. PubMed ID: 23163891 [TBL] [Abstract][Full Text] [Related]
12. A novel missense mutation of the paired box 3 gene in a Turkish family with Waardenburg syndrome type 1. Hazan F; Ozturk AT; Adibelli H; Unal N; Tukun A Mol Vis; 2013; 19():196-202. PubMed ID: 23378733 [TBL] [Abstract][Full Text] [Related]
13. Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II. Zhang H; Chen H; Luo H; An J; Sun L; Mei L; He C; Jiang L; Jiang W; Xia K; Li JD; Feng Y Hum Genet; 2012 Mar; 131(3):491-503. PubMed ID: 21965087 [TBL] [Abstract][Full Text] [Related]
14. Identification and functional analysis of a novel missense mutation of PAX3 associated with Waardenburg syndrome type I. Niu Z; Mei L; Tang F; Li J; Wang X; Sun J; He C; Cheng H; Liu Y; Cai X; Song J; Feng Y; Jiang L Eur Arch Otorhinolaryngol; 2021 Aug; 278(8):2807-2815. PubMed ID: 32940795 [TBL] [Abstract][Full Text] [Related]
15. Epistatic relationship between Waardenburg syndrome genes MITF and PAX3. Watanabe A; Takeda K; Ploplis B; Tachibana M Nat Genet; 1998 Mar; 18(3):283-6. PubMed ID: 9500554 [TBL] [Abstract][Full Text] [Related]
16. PAX3 mutations and clinical characteristics in Chinese patients with Waardenburg syndrome type 1. Wang J; Li S; Xiao X; Wang P; Guo X; Zhang Q Mol Vis; 2010 Jun; 16():1146-53. PubMed ID: 20664692 [TBL] [Abstract][Full Text] [Related]
17. Double heterozygous mutations of MITF and PAX3 result in Waardenburg syndrome with increased penetrance in pigmentary defects. Yang T; Li X; Huang Q; Li L; Chai Y; Sun L; Wang X; Zhu Y; Wang Z; Huang Z; Li Y; Wu H Clin Genet; 2013 Jan; 83(1):78-82. PubMed ID: 22320238 [TBL] [Abstract][Full Text] [Related]
18. Case Report: A Novel Hu Q; Ma H; Shen J; Zhuang Z; Li J; Huang X; Li X; Li H Front Genet; 2021; 12():609040. PubMed ID: 33747040 [No Abstract] [Full Text] [Related]
19. Mutations in PAX3 that cause Waardenburg syndrome type I: ten new mutations and review of the literature. Baldwin CT; Hoth CF; Macina RA; Milunsky A Am J Med Genet; 1995 Aug; 58(2):115-22. PubMed ID: 8533800 [TBL] [Abstract][Full Text] [Related]
20. First report of Klein-Waardenburg Syndrome in Iran and a novel pathogenic splice site variant in PAX3 gene. Saberi M; Golchehre Z; Salmani H; Karamzade A; Tabatabaie SZ; Keramatipour M Int J Pediatr Otorhinolaryngol; 2018 Oct; 113():229-233. PubMed ID: 30173992 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]