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Neil A Miller

Showing results (11-20 of 43) with videos related to

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Genome Medicine|March 31, 2012
Next-generation community genetics for low- and middle-income countriesStephen F Kingsmore, John D Lantos, Darrell L Dinwiddie, et al.
BMC Medical Genomics|September 19, 2013
De novo frameshift mutation in ASXL3 in a patient with global developmental delay, microcephaly, and craniofacial anomaliesDarrell L Dinwiddie, Sarah E Soden, Carol J Saunders, et al.
Clinical Pharmacokinetics|August 30, 2021
Physiologically Based Pharmacokinetic Modelling of Inhaled Nemiralisib: Mechanistic Components for Pulmonary Absorption, Systemic Distribution, and Oral AbsorptionNeil A Miller, Rebecca H Graves, Chris D Edwards, et al.
Genomics|May 2, 2013
Diagnosis of mitochondrial disorders by concomitant next-generation sequencing of the exome and mitochondrial genomeDarrell L Dinwiddie, Laurie D Smith, Neil A Miller, et al.
Clinical Pharmacology and Therapeutics|December 6, 2018
Pharmacogene Variation Consortium Gene Introduction: NUDT15Jun J Yang, Michelle Whirl-Carrillo, Stuart A Scott, et al.
Plos Neglected Tropical Diseases|November 5, 2010
C6/36 Aedes albopictus cells have a dysfunctional antiviral RNA interference responseDoug E Brackney, Jaclyn C Scott, Fumihiko Sagawa, et al.
Clinical Pharmacology and Therapeutics|January 15, 2021
PharmVar GeneFocus: CYP2B6Zeruesenay Desta, Ahmed El-Boraie, Li Gong, et al.
Journal of Pediatric Gastroenterology and Nutrition|September 14, 2020
ITGB2 (Integrin β2) Immunomodulatory Gene Variants in Premature Infants With Necrotizing EnterocolitisLovya George, Heather Menden, Sheng Xia, et al.
Human Mutation|April 8, 2015
Alström Syndrome: Mutation Spectrum of ALMS1Jan D Marshall, Jean Muller, Gayle B Collin, et al.
Genomics|September 5, 2013
Molecular diagnosis of infantile onset inflammatory bowel disease by exome sequencingDarrell L Dinwiddie, Julia M Bracken, Julie A Bass, et al.
Pageof 5

Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
Genome Medicine|March 31, 2012
Next-generation community genetics for low- and middle-income countriesStephen F Kingsmore, John D Lantos, Darrell L Dinwiddie, et al.
BMC Medical Genomics|September 19, 2013
De novo frameshift mutation in ASXL3 in a patient with global developmental delay, microcephaly, and craniofacial anomaliesDarrell L Dinwiddie, Sarah E Soden, Carol J Saunders, et al.
Clinical Pharmacokinetics|August 30, 2021
Physiologically Based Pharmacokinetic Modelling of Inhaled Nemiralisib: Mechanistic Components for Pulmonary Absorption, Systemic Distribution, and Oral AbsorptionNeil A Miller, Rebecca H Graves, Chris D Edwards, et al.
Genomics|May 2, 2013
Diagnosis of mitochondrial disorders by concomitant next-generation sequencing of the exome and mitochondrial genomeDarrell L Dinwiddie, Laurie D Smith, Neil A Miller, et al.
Clinical Pharmacology and Therapeutics|December 6, 2018
Pharmacogene Variation Consortium Gene Introduction: NUDT15Jun J Yang, Michelle Whirl-Carrillo, Stuart A Scott, et al.
Plos Neglected Tropical Diseases|November 5, 2010
C6/36 Aedes albopictus cells have a dysfunctional antiviral RNA interference responseDoug E Brackney, Jaclyn C Scott, Fumihiko Sagawa, et al.
Clinical Pharmacology and Therapeutics|January 15, 2021
PharmVar GeneFocus: CYP2B6Zeruesenay Desta, Ahmed El-Boraie, Li Gong, et al.
Journal of Pediatric Gastroenterology and Nutrition|September 14, 2020
ITGB2 (Integrin β2) Immunomodulatory Gene Variants in Premature Infants With Necrotizing EnterocolitisLovya George, Heather Menden, Sheng Xia, et al.
Human Mutation|April 8, 2015
Alström Syndrome: Mutation Spectrum of ALMS1Jan D Marshall, Jean Muller, Gayle B Collin, et al.
Genomics|September 5, 2013
Molecular diagnosis of infantile onset inflammatory bowel disease by exome sequencingDarrell L Dinwiddie, Julia M Bracken, Julie A Bass, et al.
Pageof 5