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The Journal of Allergy and Clinical Immunology
|
October 15, 2022
A homozygous truncating mutation of FGL2 is associated with immune dysregulation
Erin 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 myopathies
Dorota 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 Arabia
Farrukh 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 population
Sarah 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 syndrome
Anas 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 tissue
Anas M Alazami, Sarah M Al-Qattan, Eissa Faqeih, et al.
Frontiers in Immunology
|
December 6, 2021
Clinical and Immunological Features of Human BCL10 Deficiency
Blanca 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 nullizygosity
Hanif 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 tolerance
Zinan Zhang, Florian Gothe, Perrine Pennamen, et al.
Science Immunology
|
March 1, 2020
PAX1 is essential for development and function of the human thymus
Yasuhiro Yamazaki, Raul Urrutia, Luis M Franco, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 66) with videos related to
Sort By:
Page
of 7
The Journal of Allergy and Clinical Immunology
|
October 15, 2022
A homozygous truncating mutation of FGL2 is associated with immune dysregulation
Erin 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 myopathies
Dorota 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 Arabia
Farrukh 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 population
Sarah 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 syndrome
Anas 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 tissue
Anas M Alazami, Sarah M Al-Qattan, Eissa Faqeih, et al.
Frontiers in Immunology
|
December 6, 2021
Clinical and Immunological Features of Human BCL10 Deficiency
Blanca 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 nullizygosity
Hanif 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 tolerance
Zinan Zhang, Florian Gothe, Perrine Pennamen, et al.
Science Immunology
|
March 1, 2020
PAX1 is essential for development and function of the human thymus
Yasuhiro Yamazaki, Raul Urrutia, Luis M Franco, et al.
Page
of 7