Authors:
Melchionda, S
Ahituv, N
Bisceglia, L
Sobe, T
Glaser, F
Rabionet, R
Arbones, ML
Notarangelo, A
Di Iorio, E
Carella, M
Zelante, L
Estivill, X
Avraham, KB
Gasparini, P
Citation: S. Melchionda et al., MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss, AM J HU GEN, 69(3), 2001, pp. 635-640
Authors:
Sobe, T
Vreugde, S
Shahin, H
Berlin, M
Davis, N
Kanaan, M
Yaron, Y
Orr-Urtreger, A
Frydman, M
Shohat, M
Avraham, KB
Citation: T. Sobe et al., The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population, HUM GENET, 106(1), 2000, pp. 50-57
Authors:
Slor, H
Batko, S
Khan, SG
Sobe, T
Emmert, S
Khadavi, A
Frumkin, A
Busch, DB
Albert, RB
Kraemer, KH
Citation: H. Slor et al., Clinical, cellular, and molecular features of an Israeli xeroderma pigmentosum family with a frameshift mutation in the XPC gene: Sun protection prolongs life, J INVES DER, 115(6), 2000, pp. 974-980
Authors:
Sobe, T
Erlich, P
Berry, A
Korostichevsky, M
Vreugde, S
Avraham, KB
Bonne-Tanir, B
Shohat, M
Citation: T. Sobe et al., High frequency of the deafness-associated 167delT mutation in the connexin26 (GJB2) gene in Israeli Ashkenazim, AM J MED G, 86(5), 1999, pp. 499-500