Inactivating Mutations in ESCO2 Cause SC Phocomelia and Roberts Syndrome: No Phenotype-Genotype Correlation
Birgitt Schüle, Angelica Oviedo, Kathreen Johnston, Shashidhar Pai, Uta FranckeVolume:
77
Year:
2005
Language:
english
DOI:
10.1086/498695
File:
PDF, 2.25 MB
english, 2005