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	1.	Novel mutations in MYTH4-FERM domains of myosin 15 are associated with autosomal recessive nonsyndromic hearing loss. [electronic resource] by Mehregan, Hoda Mohseni, Marzieh Jalalvand, Khadijeh Arzhangi, Sanaz Nikzat, Nooshin Banihashemi, Sussan Kahrizi, Kimia Najmabadi, Hossein Producer: 20190313 In: International journal of pediatric otorhinolaryngology vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Novel Mutations in KCNQ4, LHFPL5 and COCH Genes in Iranian Families with Hearing Impairment. [electronic resource] by Mehregan, Hoda Mohseni, Marzieh Akbari, Mojdeh Jalalvand, Khadijeh Arzhangi, Sanaz Nikzat, Nooshin Kahrizi, Kimia Najmabadi, Hossein Producer: 20200720 In: Archives of Iranian medicine vol. 22 Availability: No items available. Save to lists Add to cart (remove)
	3.	Association of polymorphisms at LDLR locus with coronary artery disease independently from lipid profile. [electronic resource] by Jamaldini, Seyed Hamid Babanejad, Mojgan Mozaffari, Reza Nikzat, Nooshin Jalalvand, Khadijeh Badiei, Azadeh Sanati, Hamidreza Shakerian, Farshad Afshari, Mahdi Kahrizi, Kimia Najmabadi, Hossein Producer: 20150728 In: Acta medica Iranica vol. 52 Availability: No items available. Save to lists Add to cart (remove)
	4.	Did the GJB2 35delG mutation originate in Iran? [electronic resource] by Norouzi, Vahideh Azizi, Hiva Fattahi, Zohreh Esteghamat, Fatemehsadat Bazazzadegan, Niloofar Nishimura, Carla Nikzat, Nooshin Jalalvand, Khadijeh Kahrizi, Kimia Smith, Richard J H Najmabadi, Hossein Producer: 20120118 In: American journal of medical genetics. Part A vol. 155A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss. [electronic resource] by Davarnia, Behzad Babanejad, Mojgan Fattahi, Zohreh Nikzat, Nooshin Bazazzadegan, Niloofar Pirzade, Akbar Farajollahi, Reza Nishimura, Carla Jalalvand, Khadijeh Arzhangi, Sanaz Kahrizi, Kimia Smith, Richard J H Najmabadi, Hossein Producer: 20120522 In: International journal of pediatric otorhinolaryngology vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss. [electronic resource] by Shearer, A Eliot Hildebrand, Michael S Webster, Jennifer A Kahrizi, Kimia Meyer, Nicole C Jalalvand, Khadijeh Arzhanginy, Sanaz Kimberling, William J Stephan, Dietrich Bahlo, Melanie Smith, Richard J H Najmabadi, Hossein Producer: 20090427 In: The Laryngoscope vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS). [electronic resource] by Mohseni, Marzieh Akbari, Mojdeh Booth, Kevin T Babanejad, Mojgan Azaiez, Hela Ardalani, Fariba Arzhangi, Sanaz Jalalvand, Khadijeh Nikzat, Nooshin Ghodratpour, Fatemeh Jamali, Payman Adeli, Omid Ali Habibi, Haleh Kahrizi, Kimia Najmabadi, Hossein Producer: 20210127 In: Journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population. [electronic resource] by Fattahi, Zohreh Shearer, A Eliot Babanejad, Mojgan Bazazzadegan, Niloofar Almadani, Seyed Navid Nikzat, Nooshin Jalalvand, Khadijeh Arzhangi, Sanaz Esteghamat, Fatemehsadat Abtahi, Rezvan Azadeh, Batool Smith, Richard J H Kahrizi, Kimia Najmabadi, Hossein Producer: 20121105 In: American journal of medical genetics. Part A vol. 158A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Iranome: A catalog of genomic variations in the Iranian population. [electronic resource] by Fattahi, Zohreh Beheshtian, Maryam Mohseni, Marzieh Poustchi, Hossein Sellars, Erin Nezhadi, Sayyed Hossein Amini, Amir Arzhangi, Sanaz Jalalvand, Khadijeh Jamali, Peyman Mohammadi, Zahra Davarnia, Behzad Nikuei, Pooneh Oladnabi, Morteza Mohammadzadeh, Akbar Zohrehvand, Elham Nejatizadeh, Azim Shekari, Mohammad Bagherzadeh, Maryam Shamsi-Gooshki, Ehsan Börno, Stefan Timmermann, Bernd Haghdoost, Aliakbar Najafipour, Reza Khorram Khorshid, Hamid Reza Kahrizi, Kimia Malekzadeh, Reza Akbari, Mohammad R Najmabadi, Hossein Producer: 20200309 In: Human mutation vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Distinct genetic variation and heterogeneity of the Iranian population. [electronic resource] by Mehrjoo, Zohreh Fattahi, Zohreh Beheshtian, Maryam Mohseni, Marzieh Poustchi, Hossein Ardalani, Fariba Jalalvand, Khadijeh Arzhangi, Sanaz Mohammadi, Zahra Khoshbakht, Shahrouz Najafi, Farid Nikuei, Pooneh Haddadi, Mohammad Zohrehvand, Elham Oladnabi, Morteza Mohammadzadeh, Akbar Jafari, Mandana Hadi Akhtarkhavari, Tara Gooshki, Ehsan Shamsi Haghdoost, Aliakbar Najafipour, Reza Niestroj, Lisa-Marie Helwing, Barbara Gossmann, Yasmina Toliat, Mohammad Reza Malekzadeh, Reza Nürnberg, Peter Kahrizi, Kimia Najmabadi, Hossein Nothnagel, Michael Producer: 20200220 In: PLoS genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)