| References |
Hofker MH, et al. The X-chromosome shows less genetic variation at restriciton sites than the autosomes. Am. J. Hum. Genet. 39: 438-451, 1986. PubMed: 2876629
Francke U, et al. Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: Molecular genetic evidence for deletions. Am. J. Hum. Genet. 40: 212-227, 1987. PubMed: 2883886
Hofker MH, et al. Isolation of a random cosmid clone, CX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophy. Hum. Genet. 74: 275-279, 1986. PubMed: 2877936
M H Hofker, personal communication
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