Items where Author is "Abiri, M."

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Number of items: 7.

Article

Shafaat, M. and Alaee, M.R. and Rahmanifar, A. and Setoodeh, A. and Razzaghy-Azar, M. and Bagherian, H. and Bagheri, S.D. and Zafarghandi Motlagh, F. and Hashemi, M. and Abiri, M. and Zeinali, S. (2018) Autozygosity mapping of methylmalonic acidemia associated genes by short tandem repeat markers facilitates the identification of five novel mutations in an Iranian patient cohort. Metabolic Brain Disease, 33 (5). pp. 1689-1697.

Bahrami Zadegan, S. and Dabbagh Bagheri, S. and Joudaki, A. and Samiee Aref, M.H. and Saeidian, A.H. and Abiri, M. and Zeinali, S. (2018) Development and implementation of a novel panel consisting 20 markers for the detection of genetic causes of male infertility. Andrologia, 50 (4).

Bahrami Zadegan, S. and Dabbagh Bagheri, S. and Joudaki, A. and Samiee Aref, M.H. and Saeidian, A.H. and Abiri, M. and Zeinali, S. (2018) Development and implementation of a novel panel consisting 20 markers for the detection of genetic causes of male infertility. Andrologia, 50 (4).

Vahidnezhad, H. and Youssefian, L. and Saeidian, A.H. and Zeinali, S. and Touati, A. and Abiri, M. and Sotoudeh, S. and Norouz-zadeh, S. and Amirinezhad, N. and Mozafari, N. and Daneshpazhooh, M. and Mahmoudi, H. and Hamid, M. and Bradfield, J.P. and Kim, C.E. and Hakonarson, H. and Uitto, J. (2018) Genome-wide single nucleotide polymorphism-based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa. Experimental Dermatology.

Vahidnezhad, H. and Youssefian, L. and Saeidian, A.H. and Zeinali, S. and Touati, A. and Abiri, M. and Sotoudeh, S. and Norouz-zadeh, S. and Amirinezhad, N. and Mozafari, N. and Daneshpazhooh, M. and Mahmoudi, H. and Hamid, M. and Bradfield, J.P. and Kim, C.E. and Hakonarson, H. and Uitto, J. (2018) Genome-wide single nucleotide polymorphism-based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa. Experimental Dermatology.

Vahidnezhad, H. and Youssefian, L. and Saeidian, A.H. and Mahmoudi, H. and Touati, A. and Abiri, M. and Kajbafzadeh, A.-M. and Aristodemou, S. and Liu, L. and McGrath, J.A. and Ertel, A. and Londin, E. and Kariminejad, A. and Zeinali, S. and Fortina, P. and Uitto, J. (2018) Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy. Matrix Biology, 66. pp. 22-33.

Vahidnezhad, H. and Youssefian, L. and Saeidian, A.H. and Mahmoudi, H. and Touati, A. and Abiri, M. and Kajbafzadeh, A.-M. and Aristodemou, S. and Liu, L. and McGrath, J.A. and Ertel, A. and Londin, E. and Kariminejad, A. and Zeinali, S. and Fortina, P. and Uitto, J. (2018) Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy. Matrix Biology, 66. pp. 22-33.

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