Publication

Francke U, Ochs HD, de Martinville B, Giacalone J, Lindgren V, Disteche C, Pagon RA, Hofker MH, van Ommen GJ, Pearson PL, et al, Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome. Am J Hum Genet37:250-67 1985
PubMed ID: 4039107

Records Return:  (1) Show
 
Catalog IDGenderAge at SamplingDescription
GM07947Male14 YRMUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD