dr-w-reardon documents

Five years experience of predictive testing for myotonic dystrophy using linked DNA markers
Documents Five years experience of predictive testing for myotonic dystrophy using linked DNA markers
Autosomal recessive congenital intrauterine infection-like syndrome of microcephaly, intracranial calcification, and CNS disease
Documents Autosomal recessive congenital intrauterine infection-like syndrome of microcephaly, intracranial calcification, and CNS disease
Mesomelic limb shortness: A previously unreported autosomal recessive type
Documents Mesomelic limb shortness: A previously unreported autosomal recessive type
Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13–q21 deletion related deafness
Documents Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13–q21 deletion related deafness