Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family
Journal Article
Overview
publication date
- March 1, 2004
has subject area
- Animals
- Biological Factors - Fibroblast Growth Factor 10
- Biological Factors - Fibroblast Growth Factors
- Biological Factors - Wnt Proteins
- Biological Factors - Wnt3 Protein
- Cellular Structures - Chromosomes, Human, Pair 17
- Chromosome Mapping
- Congenital Abnormalities - Ectromelia
- Female
- Genetic Phenomena - Consanguinity
- Genetic Phenomena - Consanguinity
- Genetic Structures - Chromosomes, Human, Pair 17
- Haplotypes
- Humans
- Male
- Mice
- Musculoskeletal Diseases - Ectromelia
- Mutation
- Pedigree
- Peptides - Fibroblast Growth Factor 10
- Peptides - Fibroblast Growth Factors
- Proteins
- Proteins - Fibroblast Growth Factor 10
- Proteins - Fibroblast Growth Factors
- Proteins - Wnt Proteins
- Proteins - Wnt3 Protein
- Sequence Analysis, DNA
has restriction
- bronze
Date in CU Experts
- January 30, 2018 10:48 AM
Full Author List
- Niemann S; Zhao CF; Pascu F; Stahl U; Aulepp U; Niswander L; Weber JL; Müller U
author count
- 8
citation count
- 210
published in
Other Profiles
International Standard Serial Number (ISSN)
- 0002-9297
Digital Object Identifier (DOI)
Additional Document Info
start page
- 558
end page
- 563
volume
- 74
issue
- 3