Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome (Q35200261)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome |
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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 (English)
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U Francke
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H D Ochs
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B de Martinville
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J Giacalone
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V Lindgren
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C Distèche
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R A Pagon
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M H Hofker
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G J van Ommen
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P L Pearson
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