Prenatal diagnosis of a familial 2p16.3 deletion encompassing NRXN1 associated with no apparently phenotypic abnormality in the family carrier members.

Authors

Chih-Ping Chen

Published in

Taiwanese journal of obstetrics & gynecology. Volume 65. Issue 5. Pages 1044-1046.

PMID:
42642129
Bibliographic data and abstract were imported from PubMed on 26 Aug 2026.

Read full publication at:
Please sign in to see all details.

Stats

1-terrible, 9-excellent. How would you rate this publication? Sign in in to submit your rating.

Post a comment

You need to be signed in to post comments. You can sign in here.

Comments

There are no comments yet.