(Q42822976)
Statements
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Random X inactivation resulting in mosaic nullisomy of region Xp21.1----p21.3 associated with heterozygosity for ornithine transcarbamylase deficiency and for chronic granulomatous disease (English)
1 reference
Francke U
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1 January 1984
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1 reference
38
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4
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298-307
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Identifiers
1 reference