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Anas M Alazami

Showing results (51-60 of 66) with videos related to

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The Journal of Allergy and Clinical Immunology|October 15, 2022
A homozygous truncating mutation of FGL2 is associated with immune dysregulationErin Janssen, Mohammad F Alosaimi, Anas M Alazami, et al.
Human Genomics|September 28, 2016
A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathiesDorota Monies, Hindi N Alhindi, Mohamed A Almuhaizea, et al.
Journal of Clinical Immunology|November 8, 2022
Phenotypic and Genotypic Characterization of Hereditary Angioedema in Saudi ArabiaFarrukh Sheikh, Huda Alajlan, Maram Albanyan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 16, 2014
The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous populationSarah M Al-Qattan, Salma M Wakil, Shamsa Anazi, et al.
American Journal of Human Genetics|November 26, 2008
Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndromeAnas M Alazami, Amr Al-Saif, Abdulaziz Al-Semari, et al.
Human Genetics|March 30, 2016
Expanding the clinical and genetic heterogeneity of hereditary disorders of connective tissueAnas M Alazami, Sarah M Al-Qattan, Eissa Faqeih, et al.
Frontiers in Immunology|December 6, 2021
Clinical and Immunological Features of Human BCL10 DeficiencyBlanca Garcia-Solis, Ana Van Den Rym, Jareb J Pérez-Caraballo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 14, 2012
Autozygome maps dispensable DNA and reveals potential selective bias against nullizygosityHanif G Khalak, Salma M Wakil, Faiqa Imtiaz, et al.
The Journal of Experimental Medicine|May 2, 2019
Human interleukin-2 receptor β mutations associated with defects in immunity and peripheral toleranceZinan Zhang, Florian Gothe, Perrine Pennamen, et al.
Science Immunology|March 1, 2020
PAX1 is essential for development and function of the human thymusYasuhiro Yamazaki, Raul Urrutia, Luis M Franco, et al.
Pageof 7

Showing results (51-60 of 66) with videos related to

Sort By:
Pageof 7
The Journal of Allergy and Clinical Immunology|October 15, 2022
A homozygous truncating mutation of FGL2 is associated with immune dysregulationErin Janssen, Mohammad F Alosaimi, Anas M Alazami, et al.
Human Genomics|September 28, 2016
A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathiesDorota Monies, Hindi N Alhindi, Mohamed A Almuhaizea, et al.
Journal of Clinical Immunology|November 8, 2022
Phenotypic and Genotypic Characterization of Hereditary Angioedema in Saudi ArabiaFarrukh Sheikh, Huda Alajlan, Maram Albanyan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 16, 2014
The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous populationSarah M Al-Qattan, Salma M Wakil, Shamsa Anazi, et al.
American Journal of Human Genetics|November 26, 2008
Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndromeAnas M Alazami, Amr Al-Saif, Abdulaziz Al-Semari, et al.
Human Genetics|March 30, 2016
Expanding the clinical and genetic heterogeneity of hereditary disorders of connective tissueAnas M Alazami, Sarah M Al-Qattan, Eissa Faqeih, et al.
Frontiers in Immunology|December 6, 2021
Clinical and Immunological Features of Human BCL10 DeficiencyBlanca Garcia-Solis, Ana Van Den Rym, Jareb J Pérez-Caraballo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 14, 2012
Autozygome maps dispensable DNA and reveals potential selective bias against nullizygosityHanif G Khalak, Salma M Wakil, Faiqa Imtiaz, et al.
The Journal of Experimental Medicine|May 2, 2019
Human interleukin-2 receptor β mutations associated with defects in immunity and peripheral toleranceZinan Zhang, Florian Gothe, Perrine Pennamen, et al.
Science Immunology|March 1, 2020
PAX1 is essential for development and function of the human thymusYasuhiro Yamazaki, Raul Urrutia, Luis M Franco, et al.
Pageof 7