Screening of gene sequence variants in Saudi Arabian children with idiopathic short stature
PurposeShort stature affects approximately 2%-3% of children, representing one of the most frequent disorders for which clinical attention is sought during childhood. Despite assumed genetic heterogeneity, mutations or deletions in the short stature homeobox-containing gene (SHOX) are frequently det...
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
Korean Pediatric Society,
2017-10-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |