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Nature Genetics
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June 1, 2010
Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes
Enza Maria Valente, Clare V Logan, Soumaya Mougou-Zerelli, et al.
American Journal of Human Genetics
|
July 19, 2023
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease
Daniel G Calame, Tianyu Guo, Chen Wang, et al.
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Showing results (121-130 of 122) with videos related to
Sort By:
Page
of 13
You have reached the last page of results.
This site can display upto 122 results.
Nature Genetics
|
June 1, 2010
Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes
Enza Maria Valente, Clare V Logan, Soumaya Mougou-Zerelli, et al.
American Journal of Human Genetics
|
July 19, 2023
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease
Daniel G Calame, Tianyu Guo, Chen Wang, et al.
Page
of 13