Adel M. Ashour

Mutations in EOGT Confirm the Genetic Heterogeneity of Autosomal-Recessive Adams-Oliver Syndrome

Ranad Shaheen, Mona Aglan, Kim M. Keppler‐Noreuil et al. · The American Journal of Human Genetics · 2013 · 132 citations · Full text

Life Sciences, Genetics, Molecular Genetics +5

Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome-Osteogenesis imperfecta phenotypic spectrum

Maria Trinidad Puig-Hervás, Samia A. Temtamy, Mona Aglan et al. · Human Mutation · 2012 · 98 citations

Life Sciences, Genetics, Molecular Genetics +14

Long interspersed nuclear element-1 (LINE1)-mediated deletion ofEVC,EVC2,C4orf6, andSTK32B in Ellis–van Creveld syndrome with borderline intelligence

Samia A. Temtamy, Mona Aglan, Guido Cocchi et al. · Human Mutation · 2008 · 58 citations

Life Sciences, Genetics, Molecular Genetics +11

Adams–Oliver syndrome: further evidence of an autosomal recessive variant

Samia A. Temtamy, Mona Aglan, Adel M. Ashour et al. · Clinical Dysmorphology · 2007 · 42 citations

Life Sciences, Genetics, Pediatrics +17

Dyggve–Melchior–Clausen syndrome: Clinical, genetic, and radiological study of 15 Egyptian patients from nine unrelated families

Mona Aglan, Samia A. Temtamy, Ekram Fateen et al. · Journal of Children s Orthopaedics · 2009 · 23 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17