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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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| Pubblicato in: | Genes (Basel) |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
MDPI
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7397071/ https://ncbi.nlm.nih.gov/pubmed/32630716 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes11070736 |
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