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Medrxiv : the Preprint Server for Health Sciences
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November 24, 2025
Recessive genomic and phenotypic variation in consanguineous families with cerebral palsy
Pritha Bisarad, Yung-Chun Wang, Peter T Skidmore, et al.
Cell Reports
|
January 6, 2015
Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families
Anas M Alazami, Nisha Patel, Hanan E Shamseldin, et al.
American Journal of Human Genetics
|
May 28, 2019
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population
Dorota Monies, Mohammed Abouelhoda, Mirna Assoum, et al.
Human Genetics
|
June 11, 2017
The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes
Dorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed, et al.
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Search research articles
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Showing results (61-70 of 64) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 64 results.
Medrxiv : the Preprint Server for Health Sciences
|
November 24, 2025
Recessive genomic and phenotypic variation in consanguineous families with cerebral palsy
Pritha Bisarad, Yung-Chun Wang, Peter T Skidmore, et al.
Cell Reports
|
January 6, 2015
Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families
Anas M Alazami, Nisha Patel, Hanan E Shamseldin, et al.
American Journal of Human Genetics
|
May 28, 2019
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population
Dorota Monies, Mohammed Abouelhoda, Mirna Assoum, et al.
Human Genetics
|
June 11, 2017
The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes
Dorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed, et al.
Page
of 7