Items where Author is "Alavi, Z"

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Number of items: 1.

Sadeghian, L and Tabatabaiefar, M and Fattahi N, N and Pourreza, M and Tahmasebi, P and Alavi, Z and Hashemzadeh Chaleshtori, M (2019) Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred. Int J Pediatr Otorhinolaryngol.

This list was generated on Thu Aug 13 01:06:40 2020 IRDT.