Moien Kanaan

Moien Kanaan

Bethlehem University - Bethlehem / Palestine
Medical and Health Sciences / Medical Genetics
AD Scientific Index ID: 418063
جامعة بيت لحم
person_outline Moien Kanaan's MOST POPULAR ARTICLES
1-) A novel deletion involving the connexin-30 gene, del (GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing … Journal of medical genetics 42 (7), 588-594, 2005
2-) Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82 The American Journal of Human Genetics 87 (1), 90-94, 2010
3-) From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30 Proceedings of the National Academy of Sciences 99 (11), 7518-7523, 2002
4-) Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals The American Journal of Human Genetics 105 (2), 267-282, 2019
5-) Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families Genome biology 12, 1-11, 2011