Cynthia C. Morton

Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9.

J. Battey, F. Bieber, S. Weremowicz, 1997, Genomics.

Genomic organization, complete sequence, and chromosomal location of the gene for human eotaxin (SCYA11), an eosinophil-specific CC chemokine.

S. Weremowicz, C. Morton, A. Luster, 1997, Genomics.

RSK3 encodes a novel pp90rsk isoform with a unique N-terminal sequence: growth factor-stimulated kinase function and nuclear translocation

S. Weremowicz, C. Morton, Y. Zhao, 1995, Molecular and cellular biology.

Identification of a YAC spanning the translocation breakpoints in uterine leiomyomata, pulmonary chondroid hamartoma, and lipoma: physical mapping of the 12q14-q15 breakpoint region in uterine leiomyomata.

J. Fletcher, K. Montgomery, S. Weremowicz, 1995, Genomics.