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MINOR XP21 CHROMOSOME DELETION IN A MALE ASSOCIATED WITH EXPRESSION OF DUCHENNE MUSCULAR-DYSTROPHY, CHRONIC GRANULOMATOUS-DISEASE, RETINITIS PIGMENTOSA, AND MCLEOD SYNDROME
Author(s): FRANCKE U, OCHS HD, DEMARTINVILLE B, GIACALONE J, LINDGREN V, DISTECHE C, PAGON RA, HOFKER MH, VANOMMEN GJB, PEARSON PL, WEDGWOOD RJ
Source: AMERICAN JOURNAL OF HUMAN GENETICS    Volume: 37    Issue: 2    Pages: 250-267    Published: 1985  
Times Cited: 374     References: 64     
Document Type: Article
Language: English
Reprint Address: FRANCKE, U (reprint author), YALE UNIV, SCH MED, DEPT HUMAN GENET, NEW HAVEN, CT 06510 USA
Addresses:
1. UNIV WASHINGTON, SCH MED, DEPT PEDIAT, SEATTLE, WA 98195 USA
2. UNIV WASHINGTON, DEPT PATHOL, SEATTLE, WA 98195 USA
3. LEIDEN STATE UNIV, INST ANTHROPOGENET, 2312 AV LEIDEN, NETHERLANDS
Publisher: UNIV CHICAGO PRESS, 5720 S WOODLAWN AVE, CHICAGO, IL 60637
Subject Category: Genetics & Heredity
IDS Number: AGY59
ISSN: 0002-9297
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