Practice guidelines for the molecular analysis of Prader-Willi and Angelman syndromes
<p>Abstract</p> <p>Background</p> <p>Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are clinically distinct neurodevelopmental genetic disorders that map to 15q11-q13. The primary phenotypes are attributable to loss of expression of imprinted genes within this r...
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| Main Authors: | , , , |
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| Format: | Book |
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BMC,
2010-05-01T00:00:00Z.
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Internet
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |