Items where Author is "Ghafouri-Fard, Soudeh"

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Article

Ebadi, Nader and Javadi, Sepehr and Salmani, TayyebAli and Miryounesi, Mohammad and Yassaee, Vahid Reza and Ghafouri-Fard, Soudeh (2018) Autosomal Recessive Hypohidrotic Ectodermal Dysplasia Caused by a Novel Mutation in EDAR Gene. International Journal of Pediatrics, 6 (1). pp. 6899-6902.

Ghafouri-Fard, Soudeh and Fardaei, Majid and Tabei, Seyed Mohammad Bagher and Dianatpour, Mehdi and Miryounesi, Mohammad (2018) A CDH3 Mutation is Segregated in an Iranian Family with Congenital Hypotrichosis and Juvenile Macular Dystrophy. International Journal of Pediatrics, 6 (1). pp. 6999-7002.

Mirzajani, Sara and Mohebi, Mehdi and Miryounesi, Mohammad and Yassaee, Vahid Reza and Ghafouri-Fard, Soudeh (2018) Genetic Diagnosis if a Lethal Form of Autosomal Recessive Polycystic Kidney Disease. International Journal of Pediatrics, 6 (2). pp. 7033-7037.

Ghafouri-Fard, Soudeh and Salehpour, Shadab and Yassaee, Vahidreza and Miryounesi, Mohammad (2016) A New Nonsense Mutation in CDKL5 Gene in a Male Patient with Early Onset Refractory Epilepsy: a Case Report. International Journal of Pediatrics, 4 (2). pp. 1315-1318.

This list was generated on Fri Sep 25 04:20:40 2020 EDT.