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Fowzan S Alkuraya

Showing results (1-10 of 576) with videos related to

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Genome Medicine|June 2, 2015
Natural human knockouts and the era of genotype to phenotypeFowzan S Alkuraya
American Journal of Human Genetics|March 5, 2021
2020 Curt Stern Award address: a more perfect clinical genome-how consanguineous populations contribute to the medical annotation of the human genomeFowzan S Alkuraya
Trends in Genetics : TIG|December 16, 2014
Human knockout research: new horizons and opportunitiesFowzan S Alkuraya
American Journal of Medical Genetics. Part A|March 18, 2020
Phenotypic expansion of OTUD6B-related syndromeFowzan S Alkuraya
Current Protocols in Human Genetics|October 18, 2012
Discovery of rare homozygous mutations from studies of consanguineous pedigreesFowzan S Alkuraya
Nature Reviews. Genetics|November 6, 2021
Homozygosity mapping: a game-changer for autosomal recessive diseasesFowzan S Alkuraya
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 30, 2010
Autozygome decodedFowzan S Alkuraya
Nature|February 11, 2021
How the human genome transformed study of rare diseasesFowzan S Alkuraya
Human Genetics|August 3, 2013
The application of next-generation sequencing in the autozygosity mapping of human recessive diseasesFowzan S Alkuraya
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 18, 2025
Correspondence on "Genomic insights from a deeply phenotyped highly consanguineous neurodevelopmental disorders cohort" by Akter et alFowzan S Alkuraya
Pageof 58

Showing results (1-10 of 576) with videos related to

Sort By:
Pageof 58
Genome Medicine|June 2, 2015
Natural human knockouts and the era of genotype to phenotypeFowzan S Alkuraya
American Journal of Human Genetics|March 5, 2021
2020 Curt Stern Award address: a more perfect clinical genome-how consanguineous populations contribute to the medical annotation of the human genomeFowzan S Alkuraya
Trends in Genetics : TIG|December 16, 2014
Human knockout research: new horizons and opportunitiesFowzan S Alkuraya
American Journal of Medical Genetics. Part A|March 18, 2020
Phenotypic expansion of OTUD6B-related syndromeFowzan S Alkuraya
Current Protocols in Human Genetics|October 18, 2012
Discovery of rare homozygous mutations from studies of consanguineous pedigreesFowzan S Alkuraya
Nature Reviews. Genetics|November 6, 2021
Homozygosity mapping: a game-changer for autosomal recessive diseasesFowzan S Alkuraya
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 30, 2010
Autozygome decodedFowzan S Alkuraya
Nature|February 11, 2021
How the human genome transformed study of rare diseasesFowzan S Alkuraya
Human Genetics|August 3, 2013
The application of next-generation sequencing in the autozygosity mapping of human recessive diseasesFowzan S Alkuraya
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 18, 2025
Correspondence on "Genomic insights from a deeply phenotyped highly consanguineous neurodevelopmental disorders cohort" by Akter et alFowzan S Alkuraya
Pageof 58