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M Kirwin

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Clinical Pharmacology and Therapeutics|July 13, 2021

Key Considerations for Selecting a Genomic Decision Support Platform for Implementing PharmacogenomicsKelsey J Cook, Benjamin Q Duong, Nathan D Seligson, et al.

American Journal of Medical Genetics. Part A|May 23, 2013

Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndromeChristopher A Chapleau, Jane Lane, Susan M Kirwin, et al.

Annals of Clinical and Translational Neurology|January 9, 2020

Genome sequencing in persistently unsolved white matter disordersGuy Helman, Bryan R Lajoie, Joanna Crawford, et al.

The Journal of Clinical Endocrinology and Metabolism|October 2, 2020

Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1CFélixe Pelletier, Stefanie Perrier, Ferdy K Cayami, et al.

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Search research articles

Showing results (41-50 of 44) with videos related to

Sort By:

Pageof 5

You have reached the last page of results.This site can display upto 44 results.

Clinical Pharmacology and Therapeutics|July 13, 2021

Key Considerations for Selecting a Genomic Decision Support Platform for Implementing PharmacogenomicsKelsey J Cook, Benjamin Q Duong, Nathan D Seligson, et al.

American Journal of Medical Genetics. Part A|May 23, 2013

Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndromeChristopher A Chapleau, Jane Lane, Susan M Kirwin, et al.

Annals of Clinical and Translational Neurology|January 9, 2020

Genome sequencing in persistently unsolved white matter disordersGuy Helman, Bryan R Lajoie, Joanna Crawford, et al.

The Journal of Clinical Endocrinology and Metabolism|October 2, 2020

Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1CFélixe Pelletier, Stefanie Perrier, Ferdy K Cayami, et al.

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