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	1.	Homozygous Mutation in TWNK Cases Ataxia, Sensorineural Hearing Loss and Optic Nerve Atrophy. [electronic resource] by Jamali, Faezeh Ghaedi, Hamid Tafakhori, Abbas Alehabib, Elham Chapi, Marjan Daftarian, Narsis Darvish, Hossein Jamshidi, Javad Producer: 20200924 In: Archives of Iranian medicine vol. 22 Availability: No items available. Save to lists Add to cart (remove)
	2.	A novel mutation in SMOC1 and variable phenotypic expression in two patients with Waardenburg anophthalmia syndrome. [electronic resource] by Jamshidi, Javad Abdollahi, Shokoufeh Ghaedi, Hamid Alehabib, Elham Tafakhori, Abbas Alinaghi, Somayeh Chapi, Marjan Johari, Amir Hossein Darvish, Hossein Producer: 20180112 In: European journal of medical genetics vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	The rs1986112 Variant is Associated with Increased RAB8B Gene Expression in Schizophrenic Patients. [electronic resource] by Johari, Amir H Nejad, Farhad R Mansoori, Nader Vafaei, Fatemeh Salehi, Shima Alehabib, Elham Alinaghi, Somayeh Chapi, Marjan Jamali, Faezeh Darvish, Hossein Ghaedi, Hamid Producer: 20190903 In: Clinical laboratory vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Incomplete penetrance of [electronic resource] by Chapi, Marjan Sabbaghi, Hamideh Suri, Fatemeh Alehabib, Elham Rahimi-Aliabadi, Simin Jamali, Faezeh Jamshidi, Javad Emamalizadeh, Babak Darvish, Hossein Mirrahimi, Mehraban Ahmadieh, Hamid Daftarian, Narsis Producer: 20200403 In: Ophthalmic genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	COL18A1 is a candidate eye iridocorneal angle-closure gene in humans. [electronic resource] by Suri, Fatemeh Yazdani, Shahin Chapi, Marjan Safari, Iman Rasooli, Paniz Daftarian, Narsis Jafarinasab, Mohammad Reza Ghasemi Firouzabadi, Saghar Alehabib, Elham Darvish, Hossein Klotzle, Brandy Fan, Jian-Bing Turk, Casey Elahi, Elahe Producer: 20190422 In: Human molecular genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genes. [electronic resource] by Darvish, Hossein Azcona, Luis J Tafakhori, Abbas Mesias, Roxana Ahmadifard, Azadeh Sanchez, Elena Habibi, Arman Alehabib, Elham Johari, Amir Hossein Emamalizadeh, Babak Jamali, Faezeh Chapi, Marjan Jamshidi, Javad Kajiwara, Yuji Paisán-Ruiz, Coro Producer: 20201119 In: Scientific reports vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)