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pro vyhledávání: '"Sandra Paulina Smieszek"'
Autor:
Sandra Paulina Smieszek
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-7 (2024)
Abstract Background This study aimed to characterize the frequency of RAI1 genetic aberrations associated with Smith–Magenis syndrome (SMS), in a large cohort of autism spectrum disorder (ASD) whole-genome sequencing samples. We aimed to determine
Externí odkaz:
https://doaj.org/article/ffab8be809c2466aa63683475205287b
