Clinical Hypochondroplasia in a Family Caused by a Heterozygous Double Mutation in Fgfr3 Encoding Gly380Lys (Vol 143A, Pg 355, 2007)

AuthID
 P-003-ZG7
4
Author(s)
Almeida, M
·
Fernandes, H
·
Wilkie, A
Document Type
Correction
Year published
2008
Published
in AMERICAN JOURNAL OF MEDICAL GENETICS PART A, ISSN: 1552-4825
Volume: 146A, Issue: 9, Pages: 1234-1234 (1)
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Publication Identifiers
Scopus: 2-s2.0-43049129617
Wos: WOS:000255422900019
Source Identifiers
ISSN: 1552-4825
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