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Journal of Applied Genetics|October 7, 2022
Investigating the genetic profile of familial atypical cystic fibrosis patients (DeltaF508-CFTR) with neonatal biliary atresiaEyad Altamimi, Omar Rabab'h, Dunia Aburizeg, et al.Journal of Pediatric Gastroenterology and Nutrition|January 7, 2025
Genetic profiling of Wilson disease reveals a potential recurrent pathogenic variant of ATP7B in the Jordanian populationFareed Khdair Ahmad, Dunia Aburizeg, Yaser Rayyan, et al.Genes|June 24, 2022
Potential Composite Digenic Contribution of <i>NPC1</i> and <i>NOD2</i> Leading to Atypical Lethal Niemann-Pick Type C with Initial Crohn's Disease-like Presentation: Genotype-Phenotype Correlation StudyBilal Azab, Omar Rabab'h, Dunia Aburizeg, et al.Cancers|September 13, 2025
Histopathological, Immunohistochemical, Molecular and Genetic Biomarkers in Differentiated Thyroid CancerMousa A Al-Abbadi, Dunia Aburizeg, Husam Abuawad, et al.Genes|December 23, 2022
<i>SLC26A4</i> Phenotypic Variability Influences Intra- and Inter-Familial Diagnosis and ManagementMohamed Tawalbeh, Dunia Aburizeg, Bayan O Abu Alragheb, et al.Genes|April 30, 2021
Unique Variant Spectrum in a Jordanian Cohort with Inherited Retinal DystrophiesBilal Azab, Zain Dardas, Dunia Aburizeg, et al.Scientific Reports|July 2, 2024
Unraveling the genetic tapestry of pediatric sarcomeric cardiomyopathies and masquerading phenocopies in JordanBilal Azab, Dunia Aburizeg, Sherin T Shaaban, et al.Molecular Medicine Reports|May 6, 2022
<i>TBX5</i> variant with the novel phenotype of mixed‑type total anomalous pulmonary venous return in Holt‑Oram Syndrome and variable intrafamilial heart defectsBilal Azab, Dunia Aburizeg, Weizhen Ji, et al.Frontiers in Cell and Developmental Biology|June 18, 2026
Clinical heterogeneity associated with Bardet-Biedl syndrome-related genes in presumed non-syndromic inherited retinal diseaseBilal Azab, Dunia Aburizeg, Abdalrahman Al-Slaimieh, et al.Pageof 1