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Growth Trajectories in Genetic Subtypes of Prader–Willi Syndrome
Prader–Willi syndrome (PWS) is a rare disorder caused by the loss of expression of genes on the paternal copy of chromosome 15q11-13. The main molecular subtypes of PWS are the deletion of 15q11-13 and non-deletion, and differences in neurobehavioral phenotype are recognized between the subtypes. Th...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI AG
2020-07-01
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| Colecção: | Genes |
| Assuntos: | |
| Acesso em linha: | https://www.mdpi.com/2073-4425/11/7/736 |
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