Yazar "Schanze, D." için listeleme
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Clinical and Molecular Studies in Two Families With Fraser Syndrome: A New Fras1 Gene Mutation, Prenatal Ultrasound Findings and Implications For Genetic Counselling
Ogur, G.; Zenker, M.; Tosun, M.; Ekici, F.; Schanze, D.; Ozyilmaz, B.; Malatyalioglu, E. (Medecine Et Hygiene, 2011)Clinical and molecular studies in two families with Fraser syndrome: a new FRAS1 gene mutation, prenatal ultrasound findings and implications for genetic counselling: Fraser syndrome is a rare autosomal recessive genetic ...
