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Anas M Alazami

Showing results (21-30 of 66) with videos related to

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Frontiers in Immunology|February 16, 2024
A unique STK4 mutation truncating only the C-terminal SARAH domain results in a mild clinical phenotype despite severe T cell lymphopenia: Case reportBandar Al-Saud, Huda Alajlan, Hibah Alruwaili, et al.
American Journal of Human Genetics|September 8, 2009
FREM1 mutations cause bifid nose, renal agenesis, and anorectal malformations syndromeAnas M Alazami, Ranad Shaheen, Fatema Alzahrani, et al.
Genome Biology|November 6, 2015
TLE6 mutation causes the earliest known human embryonic lethalityAnas M Alazami, Salma M Awad, Serdar Coskun, et al.
Human Genome Variation|April 16, 2016
The many faces of KIF7Duna Barakeh, Eissa Faqeih, Shams Anazi, et al.
Scientific Reports|June 17, 2018
Deletion of DDB1- and CUL4- associated factor-17 (Dcaf17) gene causes spermatogenesis defects and male infertility in miceAsmaa Ali, Bhavesh V Mistry, Hala A Ahmed, et al.
Scientific Reports|August 3, 2018
Publisher Correction: Deletion of DDB1- and CUL4- associated factor-17 (Dcaf17) gene causes spermatogenesis defects and male infertility in miceAsmaa Ali, Bhavesh V Mistry, Hala A Ahmed, et al.
BMC Medical Genetics|July 6, 2019
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegiaSalma M Wakil, Safa Alhissi, Haya Al Dossari, et al.
American Journal of Medical Genetics. Part A|May 15, 2015
Report of a case of Raine syndrome and literature reviewMohammed Zain Seidahmed, Anas M Alazami, Omer Bashir Abdelbasit, et al.
Modern Rheumatology|February 10, 2021
Lupus manifestations in children with primary immunodeficiency diseases: Comprehensive phenotypic and genetic features and outcomeSulaiman M Al-Mayouf, Hajar A Alreefi, Tuqa A Alsinan, et al.
BMC Genomics|October 22, 2016
Impaired telomere maintenance in Alazami syndrome patients with LARP7 deficiencyBrody Holohan, Wanil Kim, Tsung-Po Lai, et al.
Pageof 7

Showing results (21-30 of 66) with videos related to

Sort By:
Pageof 7
Frontiers in Immunology|February 16, 2024
A unique STK4 mutation truncating only the C-terminal SARAH domain results in a mild clinical phenotype despite severe T cell lymphopenia: Case reportBandar Al-Saud, Huda Alajlan, Hibah Alruwaili, et al.
American Journal of Human Genetics|September 8, 2009
FREM1 mutations cause bifid nose, renal agenesis, and anorectal malformations syndromeAnas M Alazami, Ranad Shaheen, Fatema Alzahrani, et al.
Genome Biology|November 6, 2015
TLE6 mutation causes the earliest known human embryonic lethalityAnas M Alazami, Salma M Awad, Serdar Coskun, et al.
Human Genome Variation|April 16, 2016
The many faces of KIF7Duna Barakeh, Eissa Faqeih, Shams Anazi, et al.
Scientific Reports|June 17, 2018
Deletion of DDB1- and CUL4- associated factor-17 (Dcaf17) gene causes spermatogenesis defects and male infertility in miceAsmaa Ali, Bhavesh V Mistry, Hala A Ahmed, et al.
Scientific Reports|August 3, 2018
Publisher Correction: Deletion of DDB1- and CUL4- associated factor-17 (Dcaf17) gene causes spermatogenesis defects and male infertility in miceAsmaa Ali, Bhavesh V Mistry, Hala A Ahmed, et al.
BMC Medical Genetics|July 6, 2019
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegiaSalma M Wakil, Safa Alhissi, Haya Al Dossari, et al.
American Journal of Medical Genetics. Part A|May 15, 2015
Report of a case of Raine syndrome and literature reviewMohammed Zain Seidahmed, Anas M Alazami, Omer Bashir Abdelbasit, et al.
Modern Rheumatology|February 10, 2021
Lupus manifestations in children with primary immunodeficiency diseases: Comprehensive phenotypic and genetic features and outcomeSulaiman M Al-Mayouf, Hajar A Alreefi, Tuqa A Alsinan, et al.
BMC Genomics|October 22, 2016
Impaired telomere maintenance in Alazami syndrome patients with LARP7 deficiencyBrody Holohan, Wanil Kim, Tsung-Po Lai, et al.
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