Study on EcoR I fragment polymorphism of the subtelomeric domains within 4q35 and 10q26 with pulsed field gel electrophoresis in the Chinese population
FSHD associated rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit
van Deutekom JC, Wijmenga C, van Tienhoven EA, et al. FSHD associated rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit. Hum Mol Genet, 1993, 2: 2037-2042.
Genomic analysis of human chromosome 10q and 4q telomeres suggests a common origin
van Geel M, Dickson MC, Beck AF, et al. Genomic analysis of human chromosome 10q and 4q telomeres suggests a common origin. Genomics, 2002, 79: 210-217.
Interchromosomal repeat array interactions between chromosomes 4 and 10: A model for subtelomeric plasticity
van Overveld PG, Lemmers RJ, Deidda G, et al. Interchromosomal repeat array interactions between chromosomes 4 and 10:a model for subtelomeric plasticity. Hum Mol Genet, 2000, 9: 2879-2884.
Mechanism of translocation between chromosomes 4q and 10q in facioscapulohumeral muscular dystrophy
Wang N, Wu ZY, Wang CD, et al. Mechanism of translocation between chromosomes 4q and 10q in facioscapulohumeral muscular dystrophy. Natl Med J China, 2003, 83, : 650-653.
Diagnosis of facioscapulohumeral muscular dystrophy (FSHD) using double enzyme digestion associated Southern blotting method
Wang CD, Wu ZY, Wang N, et al. Diagnosis of facioscapulohumeral muscular dystrophy (FSHD) using double enzyme digestion associated Southern blotting method. Chin J Neurol, 2002, 35 : 354-356.
Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD)
Deidda G, Cacurri S, Piazzo N, et al. Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD). J Med Genet, 1996, 33: 361-365.
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females
Zatz M, Marie SK, Cerqueira A, et al. The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females. Am J Med Genet, 1998, 77: 155-161.