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Human Molecular Genetics|July 1, 1993
Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangementsM Upadhyaya, P Jardine, J Maynard, et al.
Nature Genetics|June 1, 1993
Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromsome 4q35 recombination eventsB Weiffenbach, J Dubois, D Storvick, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Endemic Tyrolean infantile cirrhosis is not an allelic variant of Wilson's diseaseC Wijmenga, T Müller, I S Murli, et al.
Genes and Immunity|July 21, 2006
Genetic variants of RANTES are associated with serum RANTES level and protection for type 1 diabetesA Zhernakova, B Z Alizadeh, P Eerligh, et al.
American Journal of Human Genetics|August 1, 1992
Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD)K A Mills, K H Buetow, Y Xu, et al.
Muscle & Nerve. Supplement|April 12, 2013
Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35C Wijmenga, H G Dauwerse, G W Padberg, et al.
Muscle & Nerve. Supplement|January 1, 1995
Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35C Wijmenga, H G Dauwerse, G W Padberg, et al.
Human Genetics|September 1, 1993
The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locusC Wijmenga, S T Winokur, G W Padberg, et al.
Human Molecular Genetics|October 1, 1993
Physical mapping and YAC-cloning connects four genetically distinct 4qter loci (D4S163, D4S139, D4F35S1 and D4F104S1) in the FSHD gene-regionC Wijmenga, T J Wright, M J Baan, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 1999
Defective collagen crosslinking in bone, but not in ligament or cartilage, in Bruck syndrome: indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17R A Bank, S P Robins, C Wijmenga, et al.
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