Sandra L. H. Davenport

Mutation of a Gene Encoding a Protein with Extracellular Matrix Motifs in Usher Syndrome Type IIa

James D. Eudy, Michael D. Weston, Su-Fang Yao et al. · Science · 1998 · 391 citations

Molecular Physiology, Developmental Biology, Markers Afm268zd1 +14

Spectrum of CHD7 Mutations in 110 Individuals with CHARGE Syndrome and Genotype-Phenotype Correlation

Seema R. Lalani, Arsalan M. Safiullah, Susan Fernbach et al. · The American Journal of Human Genetics · 2006 · 391 citations · Full text

Mendelian Disorder, Chd7 Mutations, Genetic Disorder +8

Splicing Mutations of 54-bp Exons in the COL11A1 Gene Cause Marshall Syndrome, but Other Mutations Cause Overlapping Marshall/Stickler Phenotypes

Susanna Annunen, Jarmo Körkkö, Malwina Czarny‐Ratajczak et al. · The American Journal of Human Genetics · 1999 · 258 citations · Full text

Systems Biology, Mendelian Disorder, Genetic Disorder +8

Localization of Usher syndrome type II to chromosome 1q

William J. Kimberling, Michael D. Weston, Claes Möller et al. · Genomics · 1990 · 217 citations

Medicine, Molecular Genetics, Genetics +1

Linkage of usher syndrome type I gene (USH1B) to the long arm of chromosome 11

William J. Kimberling, Claes Möller, Sandra L. H. Davenport et al. · Genomics · 1992 · 182 citations

Usher Syndrome Type, Developmental Biology, Genetic Disorder +8