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Enteric anendocrinosis attributable to a novel Neurogenin-3 variantBelal Azab, Eyad Altamimi, Omar Rabab’h et al.|European Journal of Medical Genetics|2020Cited by 7
<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, Mohamed Tawalbeh et al.|Molecular Genetics & Genomic Medicine|2020Cited by 4
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