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American Journal of Human Genetics|May 2, 2000
Candidate locus for a nuclear modifier gene for maternally inherited deafnessY Bykhovskaya, X Estivill, K Taylor, et al.
American Journal of Human Genetics|May 1, 1997
Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: frequency and differential penetrance in ovarian cancer and in breast-ovarian cancer familiesE Levy-Lahad, R Catane, S Eisenberg, et al.
Human Genetics|September 12, 2000
The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli populationT Sobe, S Vreugde, H Shahin, et al.
Dermatology (Basel, Switzerland)|January 21, 2000
Atopic dermatitis and HTLV-1-associated myelopathy: associated or coincidental disorders?M Shohat, D Ben Amitai, B Shohat, et al.
Molecular Immunology|December 1, 1990
The potential to express or suppress human interleukin-2 and interferon-gamma genes is not restricted to distinct cell subsetsM Ketzinel, G Arad, C Tal, et al.
American Journal of Medical Genetics|June 19, 1998
Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutationY Bykhovskaya, M Shohat, K Ehrenman, et al.
Clinical Genetics|June 24, 2011
High frequency of autosomal-recessive DFNB59 hearing loss in an isolated Arab population in IsraelG Borck, L Rainshtein, S Hellman-Aharony, et al.
American Journal of Medical Genetics|November 7, 1998
Correlation of linkage data with phenotype in eight families with Stickler syndromeD J Wilkin, G R Mortier, C L Johnson, et al.
Pediatrics|May 9, 2000
Familial Mediterranean fever: effects of genotype and ethnicity on inflammatory attacks and amyloidosisA Mimouni, N Magal, N Stoffman, et al.
American Journal of Medical Genetics|August 1, 1994
Desbuquois syndrome: clinical, radiographic, and morphologic characterizationM Shohat, R Lachman, H E Gruber, et al.
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