Utility of whole‐exome sequencing for patients with multiple congenital anomalies with or without intellectual disability/developmental delay in East Asia population.

Autor: Hsu, Rai‐Hseng1,2 (AUTHOR), Lee, Chen‐Hao3,4,5 (AUTHOR), Chien, Yin‐Hsiu1,2 (AUTHOR), Lin, Shuan‐Pei6,7,8 (AUTHOR), Hung, Miao‐Zi1 (AUTHOR), Chen, Nai‐Chi1 (AUTHOR), Lin, Yi‐Lin1 (AUTHOR), Hwu, Wuh‐Liang1,2 (AUTHOR), Lee, Ni‐Chung1,2 (AUTHOR) ncleentu@ntu.edu.tw
Zdroj: Molecular Genetics & Genomic Medicine. Jun2023, Vol. 11 Issue 6, p1-7. 7p.
Databáze: Academic Search Ultimate
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