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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Disease and WDR62[original query]
Molecular genetics of human primary microcephaly: an overview.
BMC medical genomics 2015 8 Suppl 1 S4.
Faheem Muhammad, Naseer Muhammad Imran, Rasool Mahmood, Chaudhary Adeel G, Kumosani Taha A, Ilyas Asad Muhammad, Pushparaj Peter, Ahmed Farid, Algahtani Hussain A, Al-Qahtani Mohammad H, Saleh Jamal Has
Diverse genetic causes of polymicrogyria with epilepsy.
Epilepsia 2021 Apr 62 (4): 973-983.
Authors are not available
WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation.
Clinical and translational medicine 2022 Jul 12 (7): e941.
Hao Lili, Ma Jing, Wu Feizhen, Ma Xiaojing, Qian Maoxiang, Sheng Wei, Yan Tizhen, Tang Ning, Jiang Xin, Zhang Bowen, Xiao Deyong, Qian Yanyan, Zhang Jin, Jiang Nan, Zhou Wenhao, Chen Weicheng, Ma Duan, Huang Guoyi
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