Confirmation of linkage of Van der Woude syndrome to chromosome 1q32: evidence of association with STR alleles suggests possible unique origin of the disease mutation. [electronic resource]

By: Contributor(s): Producer: 19991229Description: 128-34 p. digitalISSN:
  • 0270-4145
Subject(s): In: Journal of craniofacial genetics and developmental biology vol. 19
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: Journal Article; Research Support, U.S. Gov't, P.H.S.

There are no comments on this title.

to post a comment.