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Forensic Science International. Genetics
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September 11, 2015
52 additional reference population samples for the 55 AISNP panel
Andrew J Pakstis, Eva Haigh, Lotfi Cherni, et al.
Biorxiv : the Preprint Server for Biology
|
December 17, 2020
Comprehensive analysis of T cell immunodominance and immunoprevalence of SARS-CoV-2 epitopes in COVID-19 cases
Alison Tarke, John Sidney, Conner K Kidd, et al.
Cell Reports. Medicine
|
February 1, 2021
Comprehensive analysis of T cell immunodominance and immunoprevalence of SARS-CoV-2 epitopes in COVID-19 cases
Alison Tarke, John Sidney, Conner K Kidd, et al.
Science (New York, N.Y.)
|
November 19, 2005
Epidemiology. DNA identifications after the 9/11 World Trade Center attack
Leslie G Biesecker, Joan E Bailey-Wilson, Jack Ballantyne, et al.
American Journal of Human Genetics
|
August 27, 1998
Network analyses of Y-chromosomal types in Europe, northern Africa, and western Asia reveal specific patterns of geographic distribution
P Malaspina, F Cruciani, B M Ciminelli, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 25, 2008
Maternal traces of deep common ancestry and asymmetric gene flow between Pygmy hunter-gatherers and Bantu-speaking farmers
Lluís Quintana-Murci, Hélène Quach, Christine Harmant, et al.
European Journal of Human Genetics : EJHG
|
July 10, 2019
Genetic relationships of European, Mediterranean, and SW Asian populations using a panel of 55 AISNPs
Andrew J Pakstis, Cemal Gurkan, Mustafa Dogan, et al.
American Journal of Human Genetics
|
February 2, 2010
The distribution and most recent common ancestor of the 17q21 inversion in humans
Michael P Donnelly, Peristera Paschou, Elena Grigorenko, et al.
The New England Journal of Medicine
|
February 4, 2016
Vibratory Urticaria Associated with a Missense Variant in ADGRE2
Steven E Boyden, Avanti Desai, Glenn Cruse, et al.
American Journal of Human Genetics
|
June 13, 1998
OA1 mutations and deletions in X-linked ocular albinism
R E Schnur, M Gao, P A Wick, et al.
Page
of 52
Search research articles
Search
Showing results (501-510 of 516) with videos related to
Sort By:
Page
of 52
Forensic Science International. Genetics
|
September 11, 2015
52 additional reference population samples for the 55 AISNP panel
Andrew J Pakstis, Eva Haigh, Lotfi Cherni, et al.
Biorxiv : the Preprint Server for Biology
|
December 17, 2020
Comprehensive analysis of T cell immunodominance and immunoprevalence of SARS-CoV-2 epitopes in COVID-19 cases
Alison Tarke, John Sidney, Conner K Kidd, et al.
Cell Reports. Medicine
|
February 1, 2021
Comprehensive analysis of T cell immunodominance and immunoprevalence of SARS-CoV-2 epitopes in COVID-19 cases
Alison Tarke, John Sidney, Conner K Kidd, et al.
Science (New York, N.Y.)
|
November 19, 2005
Epidemiology. DNA identifications after the 9/11 World Trade Center attack
Leslie G Biesecker, Joan E Bailey-Wilson, Jack Ballantyne, et al.
American Journal of Human Genetics
|
August 27, 1998
Network analyses of Y-chromosomal types in Europe, northern Africa, and western Asia reveal specific patterns of geographic distribution
P Malaspina, F Cruciani, B M Ciminelli, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 25, 2008
Maternal traces of deep common ancestry and asymmetric gene flow between Pygmy hunter-gatherers and Bantu-speaking farmers
Lluís Quintana-Murci, Hélène Quach, Christine Harmant, et al.
European Journal of Human Genetics : EJHG
|
July 10, 2019
Genetic relationships of European, Mediterranean, and SW Asian populations using a panel of 55 AISNPs
Andrew J Pakstis, Cemal Gurkan, Mustafa Dogan, et al.
American Journal of Human Genetics
|
February 2, 2010
The distribution and most recent common ancestor of the 17q21 inversion in humans
Michael P Donnelly, Peristera Paschou, Elena Grigorenko, et al.
The New England Journal of Medicine
|
February 4, 2016
Vibratory Urticaria Associated with a Missense Variant in ADGRE2
Steven E Boyden, Avanti Desai, Glenn Cruse, et al.
American Journal of Human Genetics
|
June 13, 1998
OA1 mutations and deletions in X-linked ocular albinism
R E Schnur, M Gao, P A Wick, et al.
Page
of 52