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Nature Genetics
|
January 12, 2021
Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy
Sheng Chih Jin, Sara A Lewis, Somayeh Bakhtiari, et al.
Nature Genetics
|
September 29, 2020
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy
Sheng Chih Jin, Sara A Lewis, Somayeh Bakhtiari, 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.
JAMA Neurology
|
October 31, 2022
Genetic Testing to Inform Epilepsy Treatment Management From an International Study of Clinical Practice
Dianalee McKnight, Ana Morales, Kathryn E Hatchell, et al.
American Journal of Medical Genetics. Part A
|
January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1
Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.
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Search research articles
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Showing results (101-110 of 105) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 105 results.
Nature Genetics
|
January 12, 2021
Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy
Sheng Chih Jin, Sara A Lewis, Somayeh Bakhtiari, et al.
Nature Genetics
|
September 29, 2020
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy
Sheng Chih Jin, Sara A Lewis, Somayeh Bakhtiari, 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.
JAMA Neurology
|
October 31, 2022
Genetic Testing to Inform Epilepsy Treatment Management From an International Study of Clinical Practice
Dianalee McKnight, Ana Morales, Kathryn E Hatchell, et al.
American Journal of Medical Genetics. Part A
|
January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1
Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.
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of 11