A case of multiple congenital anomalies in association with Rett syndrome confirmed by MECP2 mutation screening. (Q52132775)
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scientific article published in July 2001
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A case of multiple congenital anomalies in association with Rett syndrome confirmed by MECP2 mutation screening. |
scientific article published in July 2001 |
Statements
A case of multiple congenital anomalies in association with Rett syndrome confirmed by MECP2 mutation screening. (English)
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Ellaway CJ
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Badawi N
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Raffaele L
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Christodoulou J
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Leonard H
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1 July 2001
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10
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3
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185-188
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