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Inactivating Mutations in ESCO2 Cause SC Phocomelia and Roberts Syndrome: No Phenotype-Genotype Correlation

Authors: Birgitt Schüle, Angélica Oviedo, Kathreen Johnston, Shashidhar Pai, Uta Francke - The American Journal of Human Genetics 2005 cited by 147

Inactivating Mutations in ESCO2 Cause SC Phocomelia and Roberts Syndrome: No Phenotype-Genotype Correlation | Litlas