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Journal of Clinical Immunology
|
December 2, 2010
ICF syndrome in Saudi Arabia: immunological, cytogenetic and molecular analysis
Namik Kaya, Saleh Al-Muhsen, Bandar Al-Saud, et al.
BMC Medical Genetics
|
January 16, 2016
A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy
Zuhair N Al-Hassnan, Zarghuna Ma Shinwari, Salma M Wakil, et al.
European Journal of Medical Genetics
|
September 16, 2008
Array comparative genomic hybridization (aCGH) reveals the largest novel deletion in PCCA found in a Saudi family with propionic acidemia
Namik Kaya, Mohammad Al-Owain, Albandary Albakheet, et al.
Mikrobiyoloji Bulteni
|
August 27, 2013
[BK virus infections in pediatric kidney transplant recipients]
Derya Mutlu, Imran Sağlık, Mustafa Koyun, et al.
Frontiers in Oncology
|
March 2, 2023
A molecular study of pediatric pilomyxoid and pilocytic astrocytomas: Genome-wide copy number screening, retrospective analysis of clinicopathological features and long-term clinical outcome
Essam AlShail, Ahmed Nasser Alahmari, Anas A M Dababo, et al.
Cell Reports
|
April 12, 2023
Circadian protein TIMELESS regulates synaptic function and memory by modulating cAMP signaling
Estibaliz Barrio-Alonso, Pablo J Lituma, Michael J Notaras, et al.
American Journal of Medical Genetics. Part A
|
December 22, 2023
Expanding the phenotypic and genotypic spectrum of GGPS1 related congenital muscular dystrophy
Ruqaiah Altassan, Hanan AlQudairy, Sarah AlJebreen, et al.
American Journal of Medical Genetics. Part A
|
March 27, 2014
Novel homozygous DEAF1 variant suspected in causing white matter disease, intellectual disability, and microcephaly
Eissa A Faqeih, Mohammed Al-Owain, Dilek Colak, et al.
Molecular Cytogenetics
|
May 28, 2019
First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient
Maysoon Alsagob, Mustafa A Salih, Muddathir H A Hamad, et al.
Dose-Response : a Publication of International Hormesis Society
|
September 1, 2023
Exposure to Cadmium Telluride Quantum Dots and Gene Expression Profile of Huh-7 Hepatocellular Carcinoma Cell Line
Hani Alothaid, Mashael R Al-Anazi, Arwa A Al-Qahtani, et al.
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Search research articles
Search
Showing results (101-110 of 145) with videos related to
Sort By:
Page
of 15
Journal of Clinical Immunology
|
December 2, 2010
ICF syndrome in Saudi Arabia: immunological, cytogenetic and molecular analysis
Namik Kaya, Saleh Al-Muhsen, Bandar Al-Saud, et al.
BMC Medical Genetics
|
January 16, 2016
A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy
Zuhair N Al-Hassnan, Zarghuna Ma Shinwari, Salma M Wakil, et al.
European Journal of Medical Genetics
|
September 16, 2008
Array comparative genomic hybridization (aCGH) reveals the largest novel deletion in PCCA found in a Saudi family with propionic acidemia
Namik Kaya, Mohammad Al-Owain, Albandary Albakheet, et al.
Mikrobiyoloji Bulteni
|
August 27, 2013
[BK virus infections in pediatric kidney transplant recipients]
Derya Mutlu, Imran Sağlık, Mustafa Koyun, et al.
Frontiers in Oncology
|
March 2, 2023
A molecular study of pediatric pilomyxoid and pilocytic astrocytomas: Genome-wide copy number screening, retrospective analysis of clinicopathological features and long-term clinical outcome
Essam AlShail, Ahmed Nasser Alahmari, Anas A M Dababo, et al.
Cell Reports
|
April 12, 2023
Circadian protein TIMELESS regulates synaptic function and memory by modulating cAMP signaling
Estibaliz Barrio-Alonso, Pablo J Lituma, Michael J Notaras, et al.
American Journal of Medical Genetics. Part A
|
December 22, 2023
Expanding the phenotypic and genotypic spectrum of GGPS1 related congenital muscular dystrophy
Ruqaiah Altassan, Hanan AlQudairy, Sarah AlJebreen, et al.
American Journal of Medical Genetics. Part A
|
March 27, 2014
Novel homozygous DEAF1 variant suspected in causing white matter disease, intellectual disability, and microcephaly
Eissa A Faqeih, Mohammed Al-Owain, Dilek Colak, et al.
Molecular Cytogenetics
|
May 28, 2019
First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient
Maysoon Alsagob, Mustafa A Salih, Muddathir H A Hamad, et al.
Dose-Response : a Publication of International Hormesis Society
|
September 1, 2023
Exposure to Cadmium Telluride Quantum Dots and Gene Expression Profile of Huh-7 Hepatocellular Carcinoma Cell Line
Hani Alothaid, Mashael R Al-Anazi, Arwa A Al-Qahtani, et al.
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of 15