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pro vyhledávání: '"A. N. Orpay"'
Publikováno v:
European Psychiatry, Vol 67, Pp S444-S445 (2024)
Introduction Smith-Magenis syndrome (SMS) is a complex genetic disorder characterised by distinctive physical features, developmental delay, cognitive impairment and a typical behavioural phenotype. SMS is caused by interstitial 17p11.2 deletions (90
Externí odkaz:
https://doaj.org/article/d4db57de798a49638fc7adfd2fe4bb2c