Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation (Q24538533)
Jump to navigation
Jump to search
scientific article
Language | Label | Description | Also known as |
---|---|---|---|
English | Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation |
scientific article |
Statements
1 reference
Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation (English)
1 reference
Birgitt Schüle
1 reference
Angelica Oviedo
1 reference
Kathreen Johnston
1 reference
Shashidhar Pai
1 reference
Uta Francke
1 reference
31 October 2005
1 reference
1 reference