Unique Variant Spectrum in a Jordanian Cohort with Inherited Retinal DystrophiesBelal Azab, Abdalla Awidi, Hana Zouk et al.|Genes|2021Cited by 9
<i>TBX5</i> variant with the novel phenotype of mixed‑type total anomalous pulmonary venous return in Holt‑Oram Syndrome and variable intrafamilial heart defectsBelal Azab, Saquib A. Lakhani, Dunia Aburizeg et al.|Molecular Medicine Reports|2022Cited by 7
Potential Composite Digenic Contribution of NPC1 and NOD2 Leading to Atypical Lethal Niemann-Pick Type C with Initial Crohn’s Disease-like Presentation: Genotype-Phenotype Correlation StudyBelal Azab, Eyad Altamimi, Dunia Aburizeg et al.|Genes|2022Cited by 4
SLC26A4 Phenotypic Variability Influences Intra- and Inter-Familial Diagnosis and ManagementMohamed Tawalbeh, Belal Azab, Dunia Aburizeg et al.|Genes|2022Cited by 4