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Anas M Alazami

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American Journal of Medical Genetics. Part A|June 17, 2008
Expanding the "E" in CHARGEAnas M Alazami, Fatema Alzahrani, Fowzan S Alkuraya
Journal of Clinical Immunology|August 21, 2020
Phenoidentical HLA-Related Hematopoietic Stem Cell Transplant Without Conditioning to Reconstitute a Patient with a Putative Loss-of-Function CARD11 MutationBashayer Al-Rasheed, Anas M Alazami, Hamoud Al-Mousa
Genomics|April 15, 2004
Human artificial chromosomes containing chromosome 17 alphoid DNA maintain an active centromere in murine cells but are not stableAnas M Alazami, José E Mejía, Zoia Larin Monaco
Neurology|May 7, 2014
SET binding factor 1 (SBF1) mutation causes Charcot-Marie-tooth disease type 4B3Anas M Alazami, Fatema Alzahrani, Saeed Bohlega, et al.
Neurogenetics|July 29, 2011
A nullimorphic ERLIN2 mutation defines a complicated hereditary spastic paraplegia locus (SPG18)Anas M Alazami, Nouran Adly, Hisham Al Dhalaan, et al.
Journal of Clinical Immunology|June 8, 2023
ZNFX1 Deficiency in a Child with Interstitial Pneumonitis and Peripheral MonocytosisBandar Al-Saud, , Turki Alshareef, et al.
Journal of Medical Genetics|January 9, 2014
NECAP1 loss of function leads to a severe infantile epileptic encephalopathyAnas M Alazami, Hadia Hijazi, Amal Y Kentab, et al.
Human Mutation|January 24, 2006
Novel PRG4 mutations underlie CACP in Saudi familiesAnas M Alazami, Sulaiman M Al-Mayouf, Carol-Ann Wyngaard, et al.
Frontiers in Immunology|February 9, 2026
Expanding the clinical spectrum of interleukin-2 receptor alpha chain deficiency: two novel cases with long-term hematopoietic stem cell transplantation outcome and literature reviewMaha Alzubedy, Ahmed Sayed Osman, Huda Alajlan, et al.
Journal of Genetics|October 7, 2015
Novel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse-Sakati syndromeMansoor C Abdulla, Anas M Alazami, Jemshad Alungal, et al.
Pageof 7

Showing results (1-10 of 66) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics. Part A|June 17, 2008
Expanding the "E" in CHARGEAnas M Alazami, Fatema Alzahrani, Fowzan S Alkuraya
Journal of Clinical Immunology|August 21, 2020
Phenoidentical HLA-Related Hematopoietic Stem Cell Transplant Without Conditioning to Reconstitute a Patient with a Putative Loss-of-Function CARD11 MutationBashayer Al-Rasheed, Anas M Alazami, Hamoud Al-Mousa
Genomics|April 15, 2004
Human artificial chromosomes containing chromosome 17 alphoid DNA maintain an active centromere in murine cells but are not stableAnas M Alazami, José E Mejía, Zoia Larin Monaco
Neurology|May 7, 2014
SET binding factor 1 (SBF1) mutation causes Charcot-Marie-tooth disease type 4B3Anas M Alazami, Fatema Alzahrani, Saeed Bohlega, et al.
Neurogenetics|July 29, 2011
A nullimorphic ERLIN2 mutation defines a complicated hereditary spastic paraplegia locus (SPG18)Anas M Alazami, Nouran Adly, Hisham Al Dhalaan, et al.
Journal of Clinical Immunology|June 8, 2023
ZNFX1 Deficiency in a Child with Interstitial Pneumonitis and Peripheral MonocytosisBandar Al-Saud, , Turki Alshareef, et al.
Journal of Medical Genetics|January 9, 2014
NECAP1 loss of function leads to a severe infantile epileptic encephalopathyAnas M Alazami, Hadia Hijazi, Amal Y Kentab, et al.
Human Mutation|January 24, 2006
Novel PRG4 mutations underlie CACP in Saudi familiesAnas M Alazami, Sulaiman M Al-Mayouf, Carol-Ann Wyngaard, et al.
Frontiers in Immunology|February 9, 2026
Expanding the clinical spectrum of interleukin-2 receptor alpha chain deficiency: two novel cases with long-term hematopoietic stem cell transplantation outcome and literature reviewMaha Alzubedy, Ahmed Sayed Osman, Huda Alajlan, et al.
Journal of Genetics|October 7, 2015
Novel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse-Sakati syndromeMansoor C Abdulla, Anas M Alazami, Jemshad Alungal, et al.
Pageof 7