| Literature DB >> 7149891 |
L Vallée, P Y Van Nerom, F G Ferraz, M Delecour, P Maroteaux, J P Farriaux, G Fontaine.
Abstract
Robinow syndrome in a mother and her 2nd male infant. Clinical and radiological findings were characteristic of this condition. Hands and spine were normal in the proband, but humerus were short. In this case, as in Robinow's first description, genetic transmission was autosomal dominant.Entities:
Mesh：
Year: 1982 PMID： 7149891
Source DB: PubMed Journal: Arch Fr Pediatr ISSN： 0003-9764