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Leukemia
|
October 14, 2020
Endemic Burkitt Lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility
Mateus H Gouveia, Isaac Otim, Martin D Ogwang, et al.
Journal of Dental Research
|
July 3, 2016
Association Studies and Direct DNA Sequencing Implicate Genetic Susceptibility Loci in the Etiology of Nonsyndromic Orofacial Clefts in Sub-Saharan African Populations
L J J Gowans, W L Adeyemo, M Eshete, et al.
American Journal of Human Genetics
|
September 13, 2011
Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection
Gaurav Bhatia, Nick Patterson, Bogdan Pasaniuc, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
November 17, 2022
Damaging Mutations in <b></b> Contribute to Risk of Nonsyndromic Cleft Lip With or Without Cleft Palate
Waheed Awotoye, Peter A Mossey, Jacqueline B Hetmanski, et al.
Scientific Reports
|
July 11, 2022
Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate
Waheed Awotoye, Peter A Mossey, Jacqueline B Hetmanski, et al.
Journal of Dental Research
|
September 9, 2017
Loss-of-Function GRHL3 Variants Detected in African Patients with Isolated Cleft Palate
M A Eshete, H Liu, M Li, et al.
Obesity (Silver Spring, Md.)
|
September 25, 2007
Meta-analysis of genome-wide linkage studies in BMI and obesity
Catherine L Saunders, Benedetta D Chiodini, Pak Sham, et al.
Diabetologia
|
August 16, 2012
Transferability and fine-mapping of glucose and insulin quantitative trait loci across populations: CARe, the Candidate Gene Association Resource
C-T Liu, M C Y Ng, D Rybin, et al.
Molecular Genetics & Genomic Medicine
|
June 20, 2020
Non-random distribution of deleterious mutations in the DNA and protein-binding domains of IRF6 are associated with Van Der Woude syndrome
Azeez A Alade, Carmen J Buxo-Martinez, Peter A Mossey, et al.
American Journal of Medical Genetics. Part A
|
March 23, 2017
22q11.2 deletion syndrome in diverse populations
Paul Kruszka, Yonit A Addissie, Daniel E McGinn, et al.
Page
of 31
Search research articles
Search
Showing results (281-290 of 302) with videos related to
Sort By:
Page
of 31
Leukemia
|
October 14, 2020
Endemic Burkitt Lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility
Mateus H Gouveia, Isaac Otim, Martin D Ogwang, et al.
Journal of Dental Research
|
July 3, 2016
Association Studies and Direct DNA Sequencing Implicate Genetic Susceptibility Loci in the Etiology of Nonsyndromic Orofacial Clefts in Sub-Saharan African Populations
L J J Gowans, W L Adeyemo, M Eshete, et al.
American Journal of Human Genetics
|
September 13, 2011
Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection
Gaurav Bhatia, Nick Patterson, Bogdan Pasaniuc, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
November 17, 2022
Damaging Mutations in <b></b> Contribute to Risk of Nonsyndromic Cleft Lip With or Without Cleft Palate
Waheed Awotoye, Peter A Mossey, Jacqueline B Hetmanski, et al.
Scientific Reports
|
July 11, 2022
Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate
Waheed Awotoye, Peter A Mossey, Jacqueline B Hetmanski, et al.
Journal of Dental Research
|
September 9, 2017
Loss-of-Function GRHL3 Variants Detected in African Patients with Isolated Cleft Palate
M A Eshete, H Liu, M Li, et al.
Obesity (Silver Spring, Md.)
|
September 25, 2007
Meta-analysis of genome-wide linkage studies in BMI and obesity
Catherine L Saunders, Benedetta D Chiodini, Pak Sham, et al.
Diabetologia
|
August 16, 2012
Transferability and fine-mapping of glucose and insulin quantitative trait loci across populations: CARe, the Candidate Gene Association Resource
C-T Liu, M C Y Ng, D Rybin, et al.
Molecular Genetics & Genomic Medicine
|
June 20, 2020
Non-random distribution of deleterious mutations in the DNA and protein-binding domains of IRF6 are associated with Van Der Woude syndrome
Azeez A Alade, Carmen J Buxo-Martinez, Peter A Mossey, et al.
American Journal of Medical Genetics. Part A
|
March 23, 2017
22q11.2 deletion syndrome in diverse populations
Paul Kruszka, Yonit A Addissie, Daniel E McGinn, et al.
Page
of 31