Christopher F. Hoth

An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome

Clinton T. Baldwin, Christopher F. Hoth, Jean Amos et al. · Nature · 1992 · 458 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I).

Christopher F. Hoth, Aubrey Milunsky, Nina R. Lipsky et al. · PubMed · 1993 · 258 citations

Expression of the Rat Adrenomedullin Receptor or a Putative Human Adrenomedullin Receptor Does Not Correlate with Adrenomedullin Binding or Functional Response

Scott P. Kennedy, Dexue Sun, Joseph J. Oleynek et al. · Biochemical and Biophysical Research Communications · 1998 · 96 citations

Adrenal Gland, Functional Response, Medicine +8

Mutations in PAX3 associated with waardenburg syndrome type I

Clinton T. Baldwin, Nina R. Lipsky, Christopher F. Hoth et al. · Human Mutation · 1994 · 75 citations

Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes.

Lindsay A. Farrer, Kathleen S. Arnos, James H. Asher et al. · PubMed · 1994 · 67 citations