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
Journal title
American journal of human genetics → ACNP
ISSN journal
00029297
Volume
37
Issue
2
Year of publication
1985
Pages
250 - 267
Database
ACNP
SICI code