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Nature Genetics
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January 12, 2023
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development
Changuk Chung, Xiaoxu Yang, Taejeong Bae, et al.
Nature Genetics
|
March 3, 2017
Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance
Ashley P L Marsh, Delphine Heron, Timothy J Edwards, et al.
American Journal of Human Genetics
|
October 9, 2021
Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss
Elodie M Richard, Somayeh Bakhtiari, Ashley P L Marsh, et al.
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Search research articles
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Showing results (11-20 of 13) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 13 results.
Nature Genetics
|
January 12, 2023
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development
Changuk Chung, Xiaoxu Yang, Taejeong Bae, et al.
Nature Genetics
|
March 3, 2017
Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance
Ashley P L Marsh, Delphine Heron, Timothy J Edwards, et al.
American Journal of Human Genetics
|
October 9, 2021
Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss
Elodie M Richard, Somayeh Bakhtiari, Ashley P L Marsh, et al.
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of 2