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Gene|November 27, 2013
Use of in silico tools for classification of novel missense mutations identified in dystrophin gene in developing countriesNarges Nouri, Esmat Fazel-Najafabadi, Mahdieh Behnam, et al.
African Journal of Traditional, Complementary, and Alternative Medicines : AJTCAM|December 7, 2013
Antispasmodic effects of yarrow (Achillea millefolium L.) extract in the isolated ileum of ratMohammad-Taghi Moradi, Mahmoud Rafieian-Koupaei, Reza Imani-Rastabi, et al.
Iranian Journal of Child Neurology|June 2, 2016
Demographic and Clinical Findings in Pediatric Patients Affected by Organic AcidemiaReza Najafi, Mahin Hashemipour, Neda Mostofizadeh, et al.
Annals of Clinical and Translational Neurology|September 28, 2019
Motor neuron diseases caused by a novel VRK1 variant - A genotype/phenotype studyMaryam Sedghi, Ali-Reza Moslemi, Montse Olive, et al.
Journal of Human Genetics|October 10, 2020
The identification of two pathogenic variants in a family with mild and severe forms of developmental delayNoriko Miyake, Shermineh Heydari, Masoud Garshasbi, et al.
Journal of Human Genetics|February 8, 2018
A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial featuresFutoshi Sekiguchi, Jafar Nasiri, Maryam Sedghi, et al.
Iranian Journal of Child Neurology|July 23, 2019
Genetic Analysis of MECP2 Gene in Iranian Patients with Rett SyndromeJafar Nasiri, Mansoor Salehi, Majid Hosseinzadeh, et al.
The American Journal of Gastroenterology|October 13, 2006
Noninvasive markers of liver fibrosis and inflammation in chronic hepatitis B-virus related liver diseaseMehdi Mohamadnejad, Ghodrat Montazeri, Atoosa Fazlollahi, et al.
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