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A Pater

Showing results (121-130 of 125) with videos related to

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Journal of Biological Methods|October 11, 2021
High throughput nanopore sequencing of SARS-CoV-2 viral genomes from patient samplesAdrian A Pater, Michael S Bosmeny, Adam A White, et al.
Biorxiv : the Preprint Server for Biology|February 9, 2026
Chemical control of 2'-hydroxyl-dependent Cas9 target engagement enables CRISPR RNA ribose replacementAdrian A Pater, Halle M Barber, Sruthi Sudhakar, et al.
Journal of Clinical Medicine|November 27, 2021
What Every Internist-Endocrinologist Should Know about Rare Genetic Syndromes in Order to Prevent Needless Diagnostics, Missed Diagnoses and Medical Complications: Five Years of 'Internal Medicine for Rare Genetic Syndromes'Anna G W Rosenberg, Minke R A Pater, Karlijn Pellikaan, et al.
Human Genetics|March 12, 2022
Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase geneJustin A Pater, Cindy Penney, Darren D O'Rielly, et al.
Human Genetics|October 11, 2021
A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) geneNelly Abdelfatah, Ahmed A Mostafa, Curtis R French, et al.
Pageof 13

Showing results (121-130 of 125) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 125 results.
Journal of Biological Methods|October 11, 2021
High throughput nanopore sequencing of SARS-CoV-2 viral genomes from patient samplesAdrian A Pater, Michael S Bosmeny, Adam A White, et al.
Biorxiv : the Preprint Server for Biology|February 9, 2026
Chemical control of 2'-hydroxyl-dependent Cas9 target engagement enables CRISPR RNA ribose replacementAdrian A Pater, Halle M Barber, Sruthi Sudhakar, et al.
Journal of Clinical Medicine|November 27, 2021
What Every Internist-Endocrinologist Should Know about Rare Genetic Syndromes in Order to Prevent Needless Diagnostics, Missed Diagnoses and Medical Complications: Five Years of 'Internal Medicine for Rare Genetic Syndromes'Anna G W Rosenberg, Minke R A Pater, Karlijn Pellikaan, et al.
Human Genetics|March 12, 2022
Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase geneJustin A Pater, Cindy Penney, Darren D O'Rielly, et al.
Human Genetics|October 11, 2021
A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) geneNelly Abdelfatah, Ahmed A Mostafa, Curtis R French, et al.
Pageof 13