Your search returned 2 results.

Results
	1.	Identification of a founder mutation for Pendred syndrome in families from northwest Iran. [electronic resource] by Mohseni, Marzieh Honarpour, Asal Mozafari, Reza Davarnia, Behzad Najmabadi, Hossein Kahrizi, Kimia Producer: 20151228 In: International journal of pediatric otorhinolaryngology vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran. [electronic resource] by Sloan-Heggen, Christina M Babanejad, Mojgan Beheshtian, Maryam Simpson, Allen C Booth, Kevin T Ardalani, Fariba Frees, Kathy L Mohseni, Marzieh Mozafari, Reza Mehrjoo, Zohreh Jamali, Leila Vaziri, Saeideh Akhtarkhavari, Tara Bazazzadegan, Niloofar Nikzat, Nooshin Arzhangi, Sanaz Sabbagh, Farahnaz Otukesh, Hasan Seifati, Seyed Morteza Khodaei, Hossein Taghdiri, Maryam Meyer, Nicole C Daneshi, Ahmad Farhadi, Mohammad Kahrizi, Kimia Smith, Richard J H Azaiez, Hela Najmabadi, Hossein Producer: 20160912 In: Journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search