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Results: 1-1 |
Results: 1
Minor Xp21 Chromosome Deletion in a Male Associated with Expression of Duchenne Muscular Dystrophy, Chronic Granulomatous Disease, Retinitis Pigmentosa, and McLeod Syndrome.
Authors: Francke, U. , Ochs, H. D. , de Martin-ville, B. , Giacalone, J. , Lindgren, V. ,
Citation: Francke, U. , Ochs, H. D. , De Martin-ville, B. , Giacalone, J. , Lindgren, V. ,, Minor Xp21 Chromosome Deletion in a Male Associated with Expression of Duchenne Muscular Dystrophy, Chronic Granulomatous Disease, Retinitis Pigmentosa, and McLeod Syndrome., American journal of human genetics , 37(2), 1985, pp. 250-267
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