Growth hormone deficiency in megalencephaly‐capillary malformation syndrome: An association with activating mutations in PIK3CA
Davis, Shanlee, Ware, Meredith A., Zeiger, Jordan, Deardorff, Matthew A., Grand, Katheryn, Grimberg, Adda, Hsu, Stephanie, Kelsey, Megan, Majidi, Shideh, Matthew, Revi P., Napier, Melanie, Nokoff, NatJournal:
American Journal of Medical Genetics Part A
DOI:
10.1002/ajmg.a.61403
Date:
November, 2019
Fichier:
PDF, 1.27 MB
2019
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