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	1.	Examination of methylation changes of [electronic resource] by Shirkavand, Atefeh Boroujeni, Zahra Niki Aleyasin, Seyed Ahmad Producer: 20190625 In: Indian journal of cancer vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	High level of intrafamilial phenotypic variability of non-syndromic hearing loss in a Lur family due to delE120 mutation in GJB2 gene. [electronic resource] by Mahdieh, Nejat Bagherian, Hamideh Shirkavand, Atefeh Sharafi, Maryam Zeinali, Sirous Producer: 20101222 In: International journal of pediatric otorhinolaryngology vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Investigation of GJB6 large deletions in Iranian patients using quantitative real-time PCR. [electronic resource] by Mahdieh, Nejat Raeisi, Marzieh Shirkavand, Atefeh Bagherian, Hamideh Akbari, Mohammad Taghi Zeinali, Sirous Producer: 20101222 In: Clinical laboratory vol. 56 Availability: No items available. Save to lists Add to cart (remove)
	4.	Unexpected heterogeneity due to recessive and de novo dominant mutations of GJB2 in an Iranian family with nonsyndromic hearing loss: implication for genetic counseling. [electronic resource] by Mahdieh, Nejat Shirkavand, Atefeh Raeisi, Marzieh Akbari, Mohammad Taghi Tekin, Mustafa Zeinali, Sirous Producer: 20101228 In: Biochemical and biophysical research communications vol. 402 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effect. [electronic resource] by Davoudi-Dehaghani, Elham Zeinali, Sirous Mahdieh, Nejat Shirkavand, Atefeh Bagherian, Hamideh Tabatabaiefar, Mohammad Amin Producer: 20131213 In: International journal of pediatric otorhinolaryngology vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Screening of OTOF mutations in Iran: a novel mutation and review. [electronic resource] by Mahdieh, Nejat Shirkavand, Atefeh Rabbani, Bahareh Tekin, Mustafa Akbari, Bahman Akbari, Mohammad Taghi Zeinali, Sirous Producer: 20130524 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)
	7.	Impact of a Missense Variation (p.S150R:AGC>AGG) in the XRCC2 Gene on Susceptibility to Colorectal Cancer. [electronic resource] by Sadat-Larijani, Mona Derakhshani, Shaghayegh Keshavarz-Pakseresht, Behta Nasri-Nasrabadi, Ali Shirkavand, Atefeh Sadat-Shandiz, Seyed Ataollah Baghbani-Arani, Fahimeh Producer: 20190909 In: Clinical laboratory vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Impact of consanguineous marriages in GJB2-related hearing loss in the Iranian population: a report of a novel variant. [electronic resource] by Mahdieh, Nejat Rabbani, Bahareh Shirkavand, Atefeh Bagherian, Hamideh Movahed, Zahra Shahab Fouladi, Paanti Rahiminejad, Faezeh Masoudifard, Masoumeh Akbari, Mohammad Taghi Zeinali, Sirous Producer: 20111115 In: Genetic testing and molecular biomarkers vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Design of a biological method for rapid detection of presence of PCR inhibitors in aged bone DNA. [electronic resource] by Ghasemi, Akram Mahdieh, Nejat Tavallaei, Mahmood Aslani, Mohammad Mehdi Zafari, Zahra Shirkavand, Atefeh Farzad, Maryam Sharafi Naderi, Mahdi Azariyan, Sajjad Habibi Zeinali, Sirous Producer: 20121015 In: Clinical laboratory vol. 58 Availability: No items available. Save to lists Add to cart (remove)
	10.	Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort. [electronic resource] by Bademci, Guney Foster, Joseph Mahdieh, Nejat Bonyadi, Mortaza Duman, Duygu Cengiz, F Basak Menendez, Ibis Diaz-Horta, Oscar Shirkavand, Atefeh Zeinali, Sirous Subasioglu, Asli Tokgoz-Yilmaz, Suna Huesca-Hernandez, Fabiola de la Luz Arenas-Sordo, Maria Dominguez-Aburto, Juan Hernandez-Zamora, Edgar Montenegro, Paola Paredes, Rosario Moreta, Germania Vinueza, Rodrigo Villegas, Franklin Mendoza-Benitez, Santiago Guo, Shengru Bozan, Nazim Tos, Tulay Incesulu, Armagan Sennaroglu, Gonca Blanton, Susan H Ozturkmen-Akay, Hatice Yildirim-Baylan, Muzeyyen Tekin, Mustafa Producer: 20161219 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)