Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance.

Por Adato, A, Kalinski, H, Weil, D, Chaib, H, Korostishevsky, M, Bonne-Tamir, B
Publicado em 1999

Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease.

Por Iyengar, S, Kalinsky, H, Weiss, S, Korostishevsky, M, Sadeh, M, Zhao, Y, Kidd, K K, Bonne-Tamir, B
Publicado em 1997

Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins.

Por Adato, A, Weil, D, Kalinski, H, Pel-Or, Y, Ayadi, H, Petit, C, Korostishevsky, M, Bonne-Tamir, B
Publicado em 1997

Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3.

Por Tamary, H, Shalmon, L, Shalev, H, Halil, A, Dobrushin, D, Ashkenazi, N, Zoldan, M, Resnitzky, P, Korostishevsky, M, Bonne-Tamir, B, Zaizov, R
Publicado em 1998

Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.

Por Bonné-Tamir, B., DeStefano, A. L., Briggs, C. E., Adair, R., Franklyn, B., Weiss, S., Korostishevsky, M., Frydman, M., Baldwin, C. T., Farrer, L. A.
Publicado em 1996