Concepedia

ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis

Amy E. Kiernan, Alexandra Erven, Stéphanie Voegeling, Jo Peters, Patrick M. Nolan, Jackie Hunter, Yvonne Bacon, Karen P. Steel, Steve D. M. Brown, Jean‐Louis Guénet

Mammalian Genome · 2002 · 47 citations · 54 references

DOI

Concepts

References

54

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

Rita Shiang, Leslie M. Thompson, Yazhen Zhu et al. · Cell · 1994 · 1.3K citations

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Defective myosin VIIA gene responsible for Usher syndrome type IB

Dominique Well, Stéphane Blanchard, Josseline Kaplan et al. · Nature · 1995 · 1.1K citations

, , +7

Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia

Francis Rousseau, Jacky Bonaventure, Laurence Legeai‐Mallet et al. · Nature · 1994 · 934 citations

, , +6

Congenital malformations of the inner ear: A classification based on embryogenesis

Robert K. Jackler, William M. Luxfor, William F. House · The Laryngoscope · 2009 · 770 citations

, , +16

A type VII myosin encoded by the mouse deafness gene shaker-1

Faith Gibson, James Walsh, Philomena Mburu et al. · Nature · 1995 · 682 citations

, , +10