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Saima Riazuddin

Showing results (131-140 of 135) with videos related to

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Journal of Medical Genetics|July 26, 2020
Otitis media susceptibility and shifts in the head and neck microbiome due to <i>SPINK5</i> variantsDaniel N Frank, Arnaud P J Giese, Lena Hafren, et al.
Human Mutation|April 23, 2019
A2ML1 and otitis media: novel variants, differential expression, and relevant pathwaysEric D Larson, Jose Pedrito M Magno, Matthew J Steritz, et al.
American Journal of Human Genetics|November 8, 2018
FUT2 Variants Confer Susceptibility to Familial Otitis MediaRegie Lyn P Santos-Cortez, Charlotte M Chiong, Daniel N Frank, et al.
American Journal of Human Genetics|August 2, 2020
De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function EffectsAndreea Manole, Stephanie Efthymiou, Emer O'Connor, 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 lossElodie M Richard, Somayeh Bakhtiari, Ashley P L Marsh, et al.
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Showing results (131-140 of 135) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 135 results.
Journal of Medical Genetics|July 26, 2020
Otitis media susceptibility and shifts in the head and neck microbiome due to <i>SPINK5</i> variantsDaniel N Frank, Arnaud P J Giese, Lena Hafren, et al.
Human Mutation|April 23, 2019
A2ML1 and otitis media: novel variants, differential expression, and relevant pathwaysEric D Larson, Jose Pedrito M Magno, Matthew J Steritz, et al.
American Journal of Human Genetics|November 8, 2018
FUT2 Variants Confer Susceptibility to Familial Otitis MediaRegie Lyn P Santos-Cortez, Charlotte M Chiong, Daniel N Frank, et al.
American Journal of Human Genetics|August 2, 2020
De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function EffectsAndreea Manole, Stephanie Efthymiou, Emer O'Connor, 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 lossElodie M Richard, Somayeh Bakhtiari, Ashley P L Marsh, et al.
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