Mordechai Shohat

发表

Mordechai Shohat, 2016 .

Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness

Mordechai Shohat, Jerome I. Rotter, K. Arnos, 1993, Nature Genetics.

Obsessive‐compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome

Abraham Weizman, Mordechai Shohat, Yehuda Finkelstein, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing

Mordechai Shohat, Serena Sirigu, Karen B Avraham, 2013, European Journal of Human Genetics.