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Prenatal and postnatal diagnosis of Phelan-McDermid syndrome: A report of 21 cases from a medical center and review… https://t.co/BO91PLDjhY #22q #22q13 #phelanmcdermidsyndrome #genetics
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RT @Spectrum: Infants with 22q13 deletions that encompass the SHANK3 gene and those with a SHANK3 mutation share a similar clinical express…
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RT @Spectrum: Infants with 22q13 deletions that encompass the SHANK3 gene and those with a SHANK3 mutation share a similar clinical express…