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The top documents tagged [novel mutation]
Prenatal Diagnosis of Complex Haemoglobinopathies Huong Le Senior Hospital Scientist Department of Molecular & Clinical Genetics Royal Prince Alfred Hospital
218 views
Database Search: Mutation Interpretation Huong Le Senior Hospital Scientist Department of Molecular & Clinical Genetics Royal Prince Alfred Hospital Sydney,
214 views
Pearls in Allergy and Immunology - February 2014
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FDA Panel Comments Adele Schneider, MD, FACMG Victor Center for the Prevention of Jewish Genetic Diseases, Director, Clinical Genetics Albert Einstein
214 views
Introduction L1 syndrome encompasses a spectrum of conditions that includes a common clinical finding of congenital hydrocephalus and X-linked inheritance
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Round and wrinkled peas
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1 Anatomy and Function of a Gene Dissection through mutation
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