- Title
- Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson—Weiss syndrome
- Creators
- Michael C GorryRobert A PrestonGregory J WhiteYingze ZhangVirender K SinghalH.Wolgang LoskenMichael G ParkerNgozi A NwokoroJ.Christopher PostGarth D Ehrlich
- Publication Details
- Human molecular genetics, v 4(8), pp 1387-1390
- Publisher
- Oxford University Press
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- Microbiology and Immunology
- Web of Science ID
- WOS:A1995RM34000019
- Scopus ID
- 2-s2.0-0029089845
- Other Identifier
- 991014878595604721
Journal article
Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson—Weiss syndrome
Human molecular genetics, v 4(8), pp 1387-1390
1995
PMID: 7581378
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- Collaboration types
- Domestic collaboration
- Web of Science research areas
- Biochemistry & Molecular Biology
- Genetics & Heredity