<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
Extending the spectrum of <i>CLRN1</i>‐ and <i>ABCA4</i>‐associated inherited retinal dystrophies caused by novel and recurrent variants using exome sequencingMohammed Abu‐Ameerh, Belal Azab, Abdalla Awidi et al.|Molecular Genetics & Genomic Medicine|2020Cited by 4
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