Search Results - "Morisot, Cyril"
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Mutations in PDGFRB Cause Autosomal-Dominant Infantile Myofibromatosis
Published in American journal of human genetics (06-06-2013)“…Infantile myofibromatosis (IM) is a disorder of mesenchymal proliferation characterized by the development of nonmetastasizing tumors in the skin, muscle,…”
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0152: Is amiodarone a safe and effective alternative drug in persistant fetal tachycardias?
Published in Archives of cardiovascular diseases supplements (01-01-2016)Get full text
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Severe combined immunodeficiency syndrome associated with autosomal recessive familial multiple gastrointestinal atresias: study of a family
Published in American journal of medical genetics (01-09-1990)“…Hereditary multiple atresias involving the gastrointestinal tract from pylorus to rectum are the most unusual form of intestinal atresia; the type of…”
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