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American Journal of Human Genetics
|
September 3, 2025
Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy
Kelsey Robinson, Sunil K Singh, Rachel B Walkup, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 4, 2026
Comprehensive analysis of <i>de novo</i> variants across 2,497 orofacial cleft trios reveals novel genetic drivers of disease
Nehir E Kurtas, Alba Sanchis-Juan, Eren Shin, et al.
Cell
|
January 7, 2022
Limb development genes underlie variation in human fingerprint patterns
Jinxi Li, James D Glover, Haiguo Zhang, et al.
Elife
|
November 26, 2019
Novel genetic loci affecting facial shape variation in humans
Ziyi Xiong, Gabriela Dankova, Laurence J Howe, et al.
Science Advances
|
February 6, 2021
A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation
Betty Bonfante, Pierre Faux, Nicolas Navarro, et al.
American Journal of Human Genetics
|
March 29, 2016
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3
Elizabeth J Leslie, Huan Liu, Jenna C Carlson, et al.
Human Molecular Genetics
|
April 2, 2016
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13
Elizabeth J Leslie, Jenna C Carlson, John R Shaffer, et al.
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of 18
Search research articles
Search
Showing results (171-180 of 177) with videos related to
Sort By:
Page
of 18
You have reached the last page of results.
This site can display upto 177 results.
American Journal of Human Genetics
|
September 3, 2025
Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy
Kelsey Robinson, Sunil K Singh, Rachel B Walkup, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 4, 2026
Comprehensive analysis of <i>de novo</i> variants across 2,497 orofacial cleft trios reveals novel genetic drivers of disease
Nehir E Kurtas, Alba Sanchis-Juan, Eren Shin, et al.
Cell
|
January 7, 2022
Limb development genes underlie variation in human fingerprint patterns
Jinxi Li, James D Glover, Haiguo Zhang, et al.
Elife
|
November 26, 2019
Novel genetic loci affecting facial shape variation in humans
Ziyi Xiong, Gabriela Dankova, Laurence J Howe, et al.
Science Advances
|
February 6, 2021
A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation
Betty Bonfante, Pierre Faux, Nicolas Navarro, et al.
American Journal of Human Genetics
|
March 29, 2016
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3
Elizabeth J Leslie, Huan Liu, Jenna C Carlson, et al.
Human Molecular Genetics
|
April 2, 2016
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13
Elizabeth J Leslie, Jenna C Carlson, John R Shaffer, et al.
Page
of 18