Author:
Barat-Houari Mouna,Nguyen Karine,Bernard Rafaëlle,Fernandez Céline,Vovan Catherine,Bareil Corinne,Van Kien Philippe Khau,Thorel Delphine,Tuffery-Giraud Sylvie,Vasseur Francis,Attarian Shahram,Pouget Jean,Girardet Anne,Lévy Nicolas,Claustres Mireille
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference45 articles.
1. Lunt PW, Compston DA, Harper PS : Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment bias. J Med Genet 1989; 26: 755–760.
2. Tonini MM, Passos-Bueno MR, Cerqueira A, Matioli SR, Pavanello R, Zatz M : Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD). Neuromuscul Disord 2004; 14: 33–38.
3. Gilbert JR, Stajich JM, Wall S et al: Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD). Am J Hum Genet 1993; 53: 401–408.
4. Mills KA, Buetow KH, Xu Y et al: Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD). Am J Hum Genet 1992; 51: 432–439.
5. Sarfarazi M, Wijmenga C, Upadhyaya M et al: Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium. Am J Hum Genet 1992; 51: 396–403.
Cited by
13 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献