Sclerosteosis-1: Clinical and Molecular Studies in an Egyptian Family
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We wrote this book for everyone looking for background genetics information about bone growth disorders especially sclerosteosis. Sclerosteosis-1 is an autosomal recessive disorder characterized by bone overgrowth due to aberrant Sclerostin protein, the product of the SOST gene. This book describes the clinical and molecular studies for the first reported affected Egyptian family with sclerosteosis-1 including novel variant and a new expanding clinical feature. I believe that the book will be a valuable resource for researchers and students looking for study of human SOST-related sclerosing bone dysplasia disorders.
Dr. Alaaeldin G. Fayez, researcher at Human Molecular Genetics. His major interests are genotyping, working on human genome sequence by bioinformatics tools, prediction of the putative effect of a new variant, molecular studies of congenital heart defects, male infertility and rare genetic diseases. He has high impact publications and memberships.
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Alaaeldin Fayez, Mona Aglan, Mona El Ruby: Sclerosteosis-1: Clinical and Molecular Studies in an Egyptian Family bei hugendubel.de. Online bestellen oder in der Filiale abholen.