Clinical characterization of autosomal dominant and recessive variants of Robinow syndrome. [electronic resource]
Producer: 20070409Description: 320-5 p. digitalISSN:- 1552-4825
- Abnormalities, Multiple -- diagnosis
- Adolescent
- Adult
- Child
- Child, Preschool
- Craniofacial Abnormalities -- diagnosis
- Diagnosis, Differential
- Female
- Genes, Dominant
- Genes, Recessive
- Genitalia -- abnormalities
- Humans
- Hypertelorism -- genetics
- Infant
- Limb Deformities, Congenital -- diagnosis
- Male
- Syndrome
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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