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Ofer Isakov

Showing results (61-70 of 67) with videos related to

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The New England Journal of Medicine|February 15, 2019
Variant <i>PADI3</i> in Central Centrifugal Cicatricial AlopeciaLiron Malki, Ofer Sarig, Maria-Teresa Romano, et al.
Human Molecular Genetics|April 11, 2015
Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT)Lonneke Haer-Wigman, Hadas Newman, Rina Leibu, et al.
Nature Genetics|August 27, 2013
Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wastingLiat Samuelov, Ofer Sarig, Robert M Harmon, et al.
The Journal of Investigative Dermatology|October 23, 2016
Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital IchthyosisRon Bochner, Liat Samuelov, Ofer Sarig, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 20, 2023
Data From a One-Stop-Shop Comprehensive Cancer Screening CenterEzra Bernstein, Shahar Lev-Ari, Shiran Shapira, et al.
Clinical Genetics|October 28, 2020
Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1Zippora Brownstein, Suleyman Gulsuner, Tom Walsh, et al.
Genome Biology|March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY ChallengeCatherine A Brownstein, Alan H Beggs, Nils Homer, et al.
Pageof 7

Showing results (61-70 of 67) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 67 results.
The New England Journal of Medicine|February 15, 2019
Variant <i>PADI3</i> in Central Centrifugal Cicatricial AlopeciaLiron Malki, Ofer Sarig, Maria-Teresa Romano, et al.
Human Molecular Genetics|April 11, 2015
Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT)Lonneke Haer-Wigman, Hadas Newman, Rina Leibu, et al.
Nature Genetics|August 27, 2013
Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wastingLiat Samuelov, Ofer Sarig, Robert M Harmon, et al.
The Journal of Investigative Dermatology|October 23, 2016
Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital IchthyosisRon Bochner, Liat Samuelov, Ofer Sarig, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 20, 2023
Data From a One-Stop-Shop Comprehensive Cancer Screening CenterEzra Bernstein, Shahar Lev-Ari, Shiran Shapira, et al.
Clinical Genetics|October 28, 2020
Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1Zippora Brownstein, Suleyman Gulsuner, Tom Walsh, et al.
Genome Biology|March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY ChallengeCatherine A Brownstein, Alan H Beggs, Nils Homer, et al.
Pageof 7