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Keith A Coffman

Showing results (11-20 of 14) with videos related to

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Molecular Genetics & Genomic Medicine|March 5, 2021
Deletion of conserved non-coding sequences downstream from NKX2-1: A novel disease-causing mechanism for benign hereditary choreaJun Liao, Keith A Coffman, Joseph Locker, et al.
Journal of Child Neurology|September 2, 2022
Deep Brain Stimulation for Pediatric Dystonia: A Review of the Literature and Suggested Programming AlgorithmRose Gelineau-Morel, Michael C Kruer, Jordan F Garris, et al.
Brain : a Journal of Neurology|August 11, 2022
Variants in the zinc transporter TMEM163 cause a hypomyelinating leukodystrophyMichelle C do Rosario, Guillermo Rodriguez Bey, Bruce Nmezi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2022
Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomesAna S A Cohen, Emily G Farrow, Ahmed T Abdelmoity, et al.
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Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Molecular Genetics & Genomic Medicine|March 5, 2021
Deletion of conserved non-coding sequences downstream from NKX2-1: A novel disease-causing mechanism for benign hereditary choreaJun Liao, Keith A Coffman, Joseph Locker, et al.
Journal of Child Neurology|September 2, 2022
Deep Brain Stimulation for Pediatric Dystonia: A Review of the Literature and Suggested Programming AlgorithmRose Gelineau-Morel, Michael C Kruer, Jordan F Garris, et al.
Brain : a Journal of Neurology|August 11, 2022
Variants in the zinc transporter TMEM163 cause a hypomyelinating leukodystrophyMichelle C do Rosario, Guillermo Rodriguez Bey, Bruce Nmezi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2022
Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomesAna S A Cohen, Emily G Farrow, Ahmed T Abdelmoity, et al.
Pageof 2