Moeenaldeen Al‐Sayed

Expanded Newborn Screening Program in Saudi Arabia: Incidence of screened disorders

Majid Alfadhel, Ali Al Othaim, Saif Al Saif et al. · Journal of Paediatrics and Child Health · 2017 · 115 citations

Medicine, Endocrinology, Pediatrics +17

Mutation of <i>HES7</i> in a large extended family with spondylocostal dysostosis and dextrocardia with <i>situs inversus</i>

Duncan B. Sparrow, Eissa Faqeih, Bahauddin Sallout et al. · American Journal of Medical Genetics Part A · 2013 · 32 citations

Life Sciences, Genetics, Molecular Genetics +12

Twenty novel mutations in BCKDHA, BCKDHB and DBT genes in a cohort of 52 Saudi Arabian patients with maple syrup urine disease

Faiqa Imtiaz, Abeer Al‐Mostafa, Rabab Allam et al. · Molecular Genetics and Metabolism Reports · 2017 · 27 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The Development of Genetic Counseling Services and Training Program in Saudi Arabia

Alya Qari, Ameera Balobaid, Rifaat Rawashdeh et al. · Journal of Genetic Counseling · 2013 · 23 citations · Full text

Life Sciences, Counselor Education, Genetics +10

Array comparative genomic hybridization (aCGH) reveals the largest novel deletion in PCCA found in a Saudi family with propionic acidemia

Namik Kaya, Mohammad Al-Owain, Albandary AlBakheet et al. · European Journal of Medical Genetics · 2008 · 14 citations

Life Sciences, Genetics, Molecular Genetics +12