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The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
March 1, 2018
Novel GREM1 Variations in Sub-Saharan African Patients With Cleft Lip and/or Cleft Palate
Lord Jephthah Joojo Gowans, Ganiyu Oseni, Peter A Mossey, et al.
Human Molecular Genetics
|
July 20, 2011
Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele
Adrienne Tin, Owen M Woodward, Wen Hong Linda Kao, et al.
Nature
|
April 13, 2021
Author Correction: High-depth African genomes inform human migration and health
Ananyo Choudhury, Shaun Aron, Laura R Botigué, et al.
Nature
|
October 29, 2020
High-depth African genomes inform human migration and health
Ananyo Choudhury, Shaun Aron, Laura R Botigué, et al.
Frontiers in Genetics
|
October 17, 2019
<i>Missense Pathogenic variants in KIF4A</i> Affect Dental Morphogenesis Resulting in X-linked Taurodontism, Microdontia and Dens-Invaginatus
Lord J J Gowans, Sophia Cameron-Christie, Rebecca L Slayton, et al.
Journal of Empirical Research on Human Research Ethics : JERHRE
|
June 30, 2025
Strengthening Research Ethics Capacity in West Africa, 2015-2024
Kyle Ferguson, Clement Adebamowo, Adebayo O Adejumo, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
August 12, 2021
Genome-Wide Scan for Parent-of-Origin Effects in a sub-Saharan African Cohort With Nonsyndromic Cleft Lip and/or Cleft Palate (CL/P)
Lord J J Gowans, Carissa L Comnick, Peter A Mossey, et al.
Molecular Genetics & Genomic Medicine
|
August 25, 2018
Identification of paternal uniparental disomy on chromosome 22 and a de novo deletion on chromosome 18 in individuals with orofacial clefts
Ganiyu O Oseni, Deepti Jain, Peter A Mossey, et al.
Human Molecular Genetics
|
February 10, 2024
The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria
Oyesola O Ojewunmi, Titilope A Adeyemo, Ajoke I Oyetunji, et al.
Leukemia
|
February 2, 2021
Author Correction to: 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.
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of 31
Search research articles
Search
Showing results (271-280 of 302) with videos related to
Sort By:
Page
of 31
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
March 1, 2018
Novel GREM1 Variations in Sub-Saharan African Patients With Cleft Lip and/or Cleft Palate
Lord Jephthah Joojo Gowans, Ganiyu Oseni, Peter A Mossey, et al.
Human Molecular Genetics
|
July 20, 2011
Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele
Adrienne Tin, Owen M Woodward, Wen Hong Linda Kao, et al.
Nature
|
April 13, 2021
Author Correction: High-depth African genomes inform human migration and health
Ananyo Choudhury, Shaun Aron, Laura R Botigué, et al.
Nature
|
October 29, 2020
High-depth African genomes inform human migration and health
Ananyo Choudhury, Shaun Aron, Laura R Botigué, et al.
Frontiers in Genetics
|
October 17, 2019
<i>Missense Pathogenic variants in KIF4A</i> Affect Dental Morphogenesis Resulting in X-linked Taurodontism, Microdontia and Dens-Invaginatus
Lord J J Gowans, Sophia Cameron-Christie, Rebecca L Slayton, et al.
Journal of Empirical Research on Human Research Ethics : JERHRE
|
June 30, 2025
Strengthening Research Ethics Capacity in West Africa, 2015-2024
Kyle Ferguson, Clement Adebamowo, Adebayo O Adejumo, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
August 12, 2021
Genome-Wide Scan for Parent-of-Origin Effects in a sub-Saharan African Cohort With Nonsyndromic Cleft Lip and/or Cleft Palate (CL/P)
Lord J J Gowans, Carissa L Comnick, Peter A Mossey, et al.
Molecular Genetics & Genomic Medicine
|
August 25, 2018
Identification of paternal uniparental disomy on chromosome 22 and a de novo deletion on chromosome 18 in individuals with orofacial clefts
Ganiyu O Oseni, Deepti Jain, Peter A Mossey, et al.
Human Molecular Genetics
|
February 10, 2024
The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria
Oyesola O Ojewunmi, Titilope A Adeyemo, Ajoke I Oyetunji, et al.
Leukemia
|
February 2, 2021
Author Correction to: 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.
Page
of 31