Smith-Lemli-Opitz syndrome: carrier frequency and spectrum of DHCR7 mutations in Canada. [electronic resource]

By: Contributor(s): Producer: 20020708Description: E31 p. digitalISSN:
  • 1468-6244
Subject(s): Online resources: In: Journal of medical genetics vol. 39
Tags from this library: No tags from this library for this title. Log in to add tags.
Star ratings
    Average rating: 0.0 (0 votes)
No physical items for this record

Publication Type: Letter; Research Support, Non-U.S. Gov't

There are no comments on this title.

to post a comment.