Maternal 21-hydroxylase deficiency and uniparental isodisomy of chromosome 6 and X results in a child with 21-hydroxylase deficiency and Klinefelter syndrome. (Q52009980)
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scientific article published in October 2006
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Maternal 21-hydroxylase deficiency and uniparental isodisomy of chromosome 6 and X results in a child with 21-hydroxylase deficiency and Klinefelter syndrome. |
scientific article published in October 2006 |
Statements
Maternal 21-hydroxylase deficiency and uniparental isodisomy of chromosome 6 and X results in a child with 21-hydroxylase deficiency and Klinefelter syndrome. (English)
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Elizabeth A Parker
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Karine Hovanes
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John Germak
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Forbes Porter
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Deborah P Merke
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1 October 2006
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140
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20
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2236-2240
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1 reference