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A J Sharp

Showing results (21-30 of 26) with videos related to

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Biorxiv : the Preprint Server for Biology|July 29, 2024
TRGT-denovo: accurate detection of <i>de novo</i> tandem repeat mutationsT Mokveld, E Dolzhenko, H Dashnow, et al.
Bioinformatics (Oxford, England)|March 24, 2019
ORE identifies extreme expression effects enriched for rare variantsF Richter, G E Hoffman, K B Manheimer, et al.
Journal of Medical Genetics|June 14, 2008
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variantF D Hannes, A J Sharp, H C Mefford, et al.
Nature Communications|December 6, 2017
Integrative transcriptomic analysis reveals key drivers of acute peanut allergic reactionsC T Watson, A T Cohain, R S Griffin, et al.
Journal of Medical Genetics|July 17, 2008
Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD A Koolen, A J Sharp, J A Hurst, et al.
Journal of Medical Genetics|April 18, 2009
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcomeB W M van Bon, H C Mefford, B Menten, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Biorxiv : the Preprint Server for Biology|July 29, 2024
TRGT-denovo: accurate detection of <i>de novo</i> tandem repeat mutationsT Mokveld, E Dolzhenko, H Dashnow, et al.
Bioinformatics (Oxford, England)|March 24, 2019
ORE identifies extreme expression effects enriched for rare variantsF Richter, G E Hoffman, K B Manheimer, et al.
Journal of Medical Genetics|June 14, 2008
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variantF D Hannes, A J Sharp, H C Mefford, et al.
Nature Communications|December 6, 2017
Integrative transcriptomic analysis reveals key drivers of acute peanut allergic reactionsC T Watson, A T Cohain, R S Griffin, et al.
Journal of Medical Genetics|July 17, 2008
Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD A Koolen, A J Sharp, J A Hurst, et al.
Journal of Medical Genetics|April 18, 2009
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcomeB W M van Bon, H C Mefford, B Menten, et al.
Pageof 3