S. Weiss

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

K. Kidd, S. Iyengar, M. Korostishevsky, 1997, Journal of medical genetics.

Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population.

K. Kidd, L. Farrer, A. De Stefano, 1995, Human molecular genetics.

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

L. Farrer, A. DeStefano, C. Baldwin, 1996, American journal of human genetics.

Genetic mapping of the gene for Usher syndrome: linkage analysis in a large Samaritan kindred.

E. Seroussi, M. Korostishevsky, V. Godel, 1994, Genomics.