Haya Levi

A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews

Israela Lerer, Michal Sagi, Ziva Ben‐Neriah et al. · Human Mutation · 2001 · 220 citations · Full text

Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delT

Israela Lerer, Michal Sagi, Esther Malamud et al. · American Journal of Medical Genetics · 2000 · 82 citations

Ashkenazi Patients, Allergy, Mendelian Disorder +13

Chromosomal Mapping and Phenotypic Characterization of Hereditary Otosclerosis Linked to the OTSC4 Locus

Zippora Brownstein, Abraham Goldfarb, Haya Levi et al. · Archives of Otolaryngology - Head and Neck Surgery · 2006 · 66 citations

Follow-Up of 40 000 Infants Screened for Hearing Defect

M. Feinmesser, Lilly Tell, Haya Levi · International Journal of Audiology · 1982 · 63 citations

Early Diagnosis, Selective Criteria, Pediatric Otolaryngology +15

Effect of Cyclosporine a on the Hearing Loss in Behçet's Disease

Josef Elidan, Évelyne Cohen, Haya Levi et al. · Annals of Otology Rhinology & Laryngology · 1991 · 55 citations