| Literature DB >> 2744039 |
D Glaser1, J Herbst, K Roggenkamp, W Tünte, W Lenz.
Abstract
We describe the clinical features of Robinow syndrome in the first child of a consanguineous Turkish couple. This observation supports the view that severe vertebral anomalies are a feature of the autosomal-recessive form of Robinow syndrome.Entities:
Mesh:
Year: 1989 PMID: 2744039 DOI: 10.1007/bf00441525
Source DB: PubMed Journal: Eur J Pediatr ISSN: 0340-6199 Impact factor: 3.183