6 research outputs found
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Recombination with pERT87 (DXS164) in families with X-linked muscular dystrophy.
No full textDystrophin expression and genotypic analysis of two cases of benign X linked myopathy (McLeod's syndrome).
No full textDNA analysis of Duchenne and Becker muscular dystrophy using pERT87 genomic probes and dystrophin cDNA probes
No full textTransient loss of proteins carrying Kell and Lutheran red cell antigens during consecutive relapses of autoimmune thrombocytopenia
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