NARA Discovery
Article Details
← Back to Search Results
Journal Article

A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects

June M. de la Cruz; Richard N. Bamford; Rebecca D. Burdine; Erich Roessler; James A. Barkovich; Dian Donnai; Alexander F. Schier; Maximilian Muenke
Human Genetics · Vol. 110, Issue 5 · pp. 422-428 · 2002

Abstract

Abstract is unavailable.

Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date2002-05-01
Publication Year2002
Volume110
Issue5
Pages422-428
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s00439-002-0709-3

Access Information

NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
Full-text access depends on NARA's subscribed coverage and institutional access.