Further elucidation of the genomic structure of PAX3, and identification of two different point mutations within the PAX3 homeobox that cause Waardenburg syndrome type 1 in two fam...

Por Lalwani, A K, Brister, J R, Fex, J, Grundfast, K M, Ploplis, B, San Agustin, T B, Wilcox, E R
Publicado em 1995

A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.

Por Lalwani, A. K., Brister, J. R., Fex, J., Grundfast, K. M., Pikus, A. T., Ploplis, B., San Agustin, T., Skarka, H., Wilcox, E. R.
Publicado em 1994