Publication
Title
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly
Author
Abstract
Language
English
Source (journal)
Journal of medical genetics. - London
Publication
London : 2013
ISSN
0022-2593
Volume/pages
50:9(2013), p. 585-592
ISI
000323450200003
Full text (Publisher's DOI)
Full text (open access)
UAntwerpen
Faculty/Department
Research group
Publication type
Subject
Affiliation
Publications with a UAntwerp address
External links
Web of Science
Record
Identification
Creation 15.10.2013
Last edited 29.01.2018
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