قسم علم الوراثة الطبية - كلية الطب
كلية الطب
Translocation t(Y;16) in a male pateint with non-obstructive azoospermia
saudi Urological association, 35th saudi Urological association, 2024
Transplantation of hyaluronic acid and menstrual blood-derived stem cells accelerated wound healing in a diabetic rat model
ScienceDirect, Tissue and Cell, 2024
Impact of rs599839 Polymorphism on Coronary Artery Disease Risk in Saudi Diabetic Patients
Wiley, Disease Markers, 2024
Influence of matrix metalloproteinase 9 variant rs17576 on ischemic stroke risk and severity in acute coronary syndrome
ScienceDirect, Journal of Stroke and Cerebrovascular Diseases, 2024
Partial trisomy 19p: Case report and a literature review”
European Human Genetics Conference 2023, European Human Genetics Conference 2023, 2024
Mosaic mutation in androgen receptor gene in a patient with partial androgen insensitivity syndrome
European Human Genetics Conference 2022, European Human Genetics Conference 2022, 2023
Heterozygous mutation in SCRIB gene in adult patient with myelomeningocele and primary infertility
European Human Genetics Virtual Conference 2021, European Human Genetics Virtual Conference 2021, 2583
Phenotypic variability to medication management: an update on fragile X syndrome.
BMC, Human Genomics, 2584
Sequence Variants in PSMB8/PSMB9 Immunoproteasome Genes and Risk of Urothelial Bladder Carcinoma
SPRINGERNATURE, CUREUS JOURNAL OF MEDICAL SCIENCE, 2584
Reciprocal Translocation T(Y;16) in a Male Patient With Non-obstructive Azoospermia: A Case Report and Literature Review
SPRINGERNATURE, CUREUS JOURNAL OF MEDICAL SCIENCE, 2583
Androgen Receptor Gene Mosaicism in Partial Androgen Insensitivity Syndrome Patient Detected
Hilaris, Clinical Case Reports, 2584
Combined genetic approaches yield a 48% diagnostic rate in a large cohort of French hearing-impaired patients
Springer Nature, Springer Nature, 2018