References | Year | PubMed Id |
| Uchitel, O.; Engel, A. G.; Walls, T. J.; Nagel, A.; Atassi, M. Z.; Bril, V. : Congenital myasthenic syndromes: II: syndrome attributed to abnormal interaction of acetylcholine with its receptor. Muscle Nerve 16: 1293-1301, 1993. | ||
| Upadhyaya M, Lunt P, Sarfarazi M, Broadhead W, Farnham J, Harper PS. The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD). Am J Hum Genet. 1992 Aug;51(2):404-10. | ||
| Upadhyaya M, Lunt PW, Sarfarazi M, Broadhead W, Daniels J, Owen M, Harper PS. DNA marker applicable to presymptomatic and prenatal diagnosis of facioscapulohumeral disease. Lancet. 1990 Nov 24;336(8726):1320-1. |