Zobrazeno 1 - 10
of 12
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
Autor:
Smieszek, Sandra Paulina1 (AUTHOR) sandra.smieszek@vandapharma.com
Publikováno v:
Egyptian Journal of Medical Human Genetics. 5/3/2024, Vol. 25 Issue 1, p1-7. 7p.
Publikováno v:
Trends Magazine. May2024, Vol. 22 Issue 5, p46-52. 7p.
Autor:
Gemmati, Donato, Longo, Giovanna, Gallo, Ines, Silva, Juliana Araujo, Secchiero, Paola, Zauli, Giorgio, Hanau, Stefania, Passaro, Angelina, Pellegatti, Patrizia, Pizzicotti, Stefano, Serino, Maria Luisa, Singh, Ajay Vikram, Tisato, Veronica
Publikováno v:
Frontiers in Genetics; 11/30/2022, Vol. 13, p1-19, 19p
Publikováno v:
Frontiers in Genetics; 9/20/2022, Vol. 13, p1-8, 8p
Autor:
Kamel, Walaa A., Kamel, Mohmed I., Alhasawi, Almunther, Elmasry, Sameh, AlHamdan, Fajer, Al-Hashel, Jasem Y.
Publikováno v:
Frontiers in Neurology; 10/7/2021, Vol. 12, p1-7, 7p