The Origin of Efnb1 Mutations in Craniofrontonasal Syndrome: Frequent Somatic Mosaicism and Explanation of the Paucity of Carrier Males

AuthID
 P-004-K8V
16
Author(s)
Twigg, SRF
·
Matsumoto, K
·
Kidd, AMJ
·
Goriely, A
·
Taylor, IB
·
Fisher, RB
·
Mathijssen, IMJ
·
Lourenco, MT
·
Sweeney, E
·
Wilson, LC
·
Mulliken, JB
·
Wall, SA
·
Wilkie, AOM
Document Type
Article
Year published
2006
Published
in AMERICAN JOURNAL OF HUMAN GENETICS, ISSN: 0002-9297
Volume: 78, Issue: 6, Pages: 999-1010 (12)
Indexing
Wos®
Scopus®
Crossref®
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 16685650
Scopus: 2-s2.0-33646879391
Wos: WOS:000237553800009
Source Identifiers
ISSN: 0002-9297
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