Rhizomelic chondrodysplasia punctata and survival beyond one year: a review of the literature and five case reports

Author:

Wardinsky T. D.,Pagon R. A.,Powell B. R.,McGillivray B.,Stephan M.,Zonana J.,Moser A.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference21 articles.

1. Chondrodysplasia punctata: report of two cases;Andersen;Skeletal Radiol.,1987

2. Chondrodysplasia punctata;Boron;Monatsschr. Kinderheilkd,1980

3. Mesomelic dysplasia with punctate epiphyseal calcifications, a new enity of chondrodysplasia punctata;Burck;Eur. J. Pediatr.,1982

4. Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X-chromosome;Curry;N. Engl. J. Med.,1984

5. Rhizomelic form of chondrodysplasia punctata;Farbis;Minerva Pediatr.,1981

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