Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenita
- 1 February 1991
- journal article
- case report
- Published by Springer Nature in Human Genetics
- Vol. 86 (4), 414-415
- https://doi.org/10.1007/bf00201848
Abstract
No abstract availableKeywords
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