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Radiology Case Reports|November 17, 2025
Placenta percreta complicated by active bleeding detected on MRI: A case reportFatima Abdulmohsen Al-Shaikh, Ibrahim Al-AbdulkareemCases Journal|October 16, 2009
Homozygous R396H mutation of the RAG1 gene in a Saudi infant with Omenn's syndrome: a case reportMohammed Al Balwi, Sulaiman Al Ajaji, Ibrahim Al Abdulkareem, et al.American Journal of Medical Genetics. Part A|August 21, 2012
A novel mutation in the SHH long-range regulator (ZRS) is associated with preaxial polydactyly, triphalangeal thumb, and severe radial ray deficiencyMohammad M Al-Qattan, Ibrahim Al Abdulkareem, Yazied Al Haidan, et al.American Journal of Medical Genetics. Part A|February 24, 2011
A novel homozygous missense mutation (c.610G>A, p.Gly204Ser) in the WNT7A gene causes tetra-amelia in two Saudi familiesWafaa Eyaid, Mohammad M Al-Qattan, Ibrahim Al Abdulkareem, et al.Molecular Genetics & Genomic Medicine|September 5, 2022
Spinal muscular atrophy carrier frequency in Saudi ArabiaMohammed Al Jumah, Saad Al Rajeh, Wafaa Eyaid, et al.Cancer Genetics|March 13, 2016
Clinical characteristics and genetic subtypes of Fanconi anemia in Saudi patientsYahya Ghazwani, Mohammed AlBalwi, Ibrahim Al-Abdulkareem, et al.Cytokine|June 28, 2014
Monomeric C-reactive protein and Notch-3 co-operatively increase angiogenesis through PI3K signalling pathwayEmhamed Boras, Mark Slevin, M Yvonne Alexander, et al.Journal of Medical Genetics|September 26, 2013
Genome-wide association study of chronic hepatitis B virus infection reveals a novel candidate risk allele on 11q22.3Ahmed Al-Qahtani, Hanif G Khalak, Fowzan S Alkuraya, et al.American Journal of Human Genetics|November 27, 2012
Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegiaChristelle Tesson, Magdalena Nawara, Mustafa A M Salih, et al.Pageof 1