DNA Sequence Fragment Containing C to A Mutation as a Convenient Mutation Standard for DHPLC Analysis

Por Dastsooz, Hassan, Vahedi, Nazanin, Fardaei, Majid
Publicado em 2013

A Novel Missense Mutation in CLCN1 Gene in a Family with Autosomal Recessive Congenital Myotonia

Por Miryounesi, Mohammad, Ghafouri-Fard, Soudeh, Fardaei, Majid
Publicado no Iran J Med Sci (2016)

Expression Analysis of Multiple Genes May Involve in Antimony Resistance among Leishmania major Clinical Isolates from Fars Province, Central Iran

Por GHOBAKHLOO, Nafiseh, MOTAZEDIAN, Mohammad Hossein, FARDAEI, Majid
Publicado no Iran J Parasitol (2016)

MSX1 Mutation in Witkop Syndrome; A Case Report

Por Ghaderi, Faezeh, Hekmat, Somaye, Ghaderi, Reza, Fardaei, Majid
Publicado em 2013

Mutation analysis of the CTNS gene in Iranian patients with infantile nephropathic cystinosis: identification of two novel mutations

Por Sadeghipour, Forough, Basiratnia, Mitra, Derakhshan, Ali, Fardaei, Majid
Publicado no Hum Genome Var (2017)

Autosomal Recessive Nonsyndromic Hearing Loss: A Case Report with a Mutation in TRIOBP Gene

Por Fardaei, Majid, Sarrafzadeh, Shaghayegh, Ghafouri-Fard, Soudeh, Miryounesi, Mohammad
Publicado no Int J Mol Cell Med (2015)

In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts

Por Fardaei, Majid, Larkin, Ken, Brook, J. David, Hamshere, Marion G.
Publicado em 2001

Limb Girdle Muscular Dystrophy Type 2E Due to a Novel Large Deletion in SGCB Gene

Por GHAFOURI-FARD, Soudeh, HASHEMI-GORJI, Feyzollah, FARDAEI, Majid, MIRYOUNESI, Mohammad
Publicado no Iran J Child Neurol (2017)

VSX1 and SOD1 Mutation Screening in Patients with Keratoconus in the South of Iran

Por Nejabat, Mahmood, Naghash, Payam, Dastsooz, Hassan, Mohammadi, Sanaz, Alipour, Mohsen, Fardaei, Majid
Publicado no J Ophthalmic Vis Res (2017)

Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports

Por Dastsooz, Hassan, Nemati, Hamid, Fard, Mohammad Ali Farazi, Fardaei, Majid, Faghihi, Mohammad Ali
Publicado no BMC Med Genet (2017)

Multiplex ARMS PCR to Detect 8 Common Mutations of ATP7B Gene in Patients With Wilson Disease

Por Dastsooz, Hassan, Imanieh, Mohammad Hadi, Dehghani, Seyed Mohsen, Haghighat, Mahmood, Moini, Maryam, Fardaei, Majid
Publicado em 2013

A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome

Por Taghdiri, Maryam, Dastsooz, Hassan, Fardaei, Majid, Mohammadi, Sanaz, Farazi Fard, Mohammad Ali, Faghihi, Mohammad Ali
Publicado no Front Pediatr (2017)

Two novel mutations in the KHDC3L gene in Asian patients with recurrent hydatidiform mole

Por Rezaei, Maryam, Nguyen, Ngoc Minh Phuong, Foroughinia, Leila, Dash, Pratima, Ahmadpour, Fatemeh, Verma, Ishwar Chandra, Slim, Rima, Fardaei, Majid
Publicado no Hum Genome Var (2016)

Muscleblind-Like Proteins : Similarities and Differences in Normal and Myotonic Dystrophy Muscle

Por Holt, Ian, Jacquemin, Virginie, Fardaei, Majid, Sewry, Caroline A., Butler-Browne, Gillian S., Furling, Denis, Brook, J. David, Morris, Glenn E.
Publicado em 2009

Auricular or body acupuncture: which one is more effective in reducing abdominal fat mass in Iranian men with obesity: a randomized clinical trial

Por Darbandi, Mahsa, Darbandi, Sara, Owji, Ali Akbar, Mokarram, Pooneh, Mobarhan, Majid Ghayor, Fardaei, Majid, Zhao, Baxiao, Abdi, Hamid, Nematy, Mohsen, Safarian, Mohammad, Parizadeh, Mohammad Reza, Dabbaghmanesh, Mohammad Hossein, Abbasi, Parisa, Ferns, Gordon
Publicado no J Diabetes Metab Disord (2014)

The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions

Por Reddy, Ramesh, Nguyen, Ngoc M P, Sarrabay, Guillaume, Rezaei, Maryam, Rivas, Mayra C G, Kavasoglu, Aysenur, Berkil, Hakan, Elshafey, Alaa, Abdalla, Ebtesam, Nunez, Kristin P, Dreyfus, Hélène, Philippe, Merviel, Hadipour, Zahra, Durmaz, Asude, Eaton, Erin E, Schubert, Brittany, Ulker, Volkan, Hadipour, Fatemeh, Touitou, Isabelle, Fardaei, Majid, Slim, Rima
Publicado no Eur J Hum Genet (2016)

The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions

Por Reddy, Ramesh, Nguyen, Ngoc M P, Sarrabay, Guillaume, Rezaei, Maryam, Rivas, Mayra C G, Kavasoglu, Aysenur, Berkil, Hakan, Elshafey, Alaa, Nunez, Kristin P, Dreyfus, Hélène, Philippe, Merviel, Hadipour, Zahra, Durmaz, Asude, Eaton, Erin E, Schubert, Brittany, Ulker, Volkan, Hadipour, Fatemeh, Ahmadpour, Fatemeh, Touitou, Isabelle, Fardaei, Majid, Slim, Rima
Publicado no Eur J Hum Genet (2016)