Resultados de búsqueda - Silawi, Mohammad

Molecular diagnostic assays for COVID-19: an overview por Habibzadeh, Parham, Mofatteh, Mohammad, Silawi, Mohammad, Ghavami, Saeid, Faghihi, Mohammad Ali

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Association between rs2303861 polymorphism in CD82 gene and non-alcoholic fatty liver disease: a preliminary case-control study por Habibzadeh, Parham, Honarvar, Behnam, Silawi, Mohammad, Bahramjahan, Shima, Kazemi, Azar, Faghihi, Mohammad Ali, Lankarani, Kamran

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Splicing defect in FKBP10 gene causes autosomal recessive osteogenesis imperfecta disease: a case report por Maghami, Fatemeh, Tabei, Seyed Mohammad Bagher, Moravej, Hossein, Dastsooz, Hassan, Modarresi, Farzaneh, Silawi, Mohammad, Faghihi, Mohammad Ali

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Clinical and molecular characterization of a patient with mitochondrial Neurogastrointestinal Encephalomyopathy por Habibzadeh, Parham, Silawi, Mohammad, Dastsooz, Hassan, Bahramjahan, Shima, Ezzatzadegan Jahromi, Shahrokh, Ostovan, Vahid Reza, Yavarian, Majid, Mofatteh, Mohammad, Faghihi, Mohammad Ali

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A novel splice site mutation in WAS gene in patient with Wiskott-Aldrich syndrome and chronic colitis: a case report por Esmaeilzadeh, Hossein, Bordbar, Mohammad Reza, Dastsooz, Hassan, Silawi, Mohammad, Fard, Mohammad Ali Farazi, Adib, Ali, Kafashan, Ali, Tabatabaei, Zahra, Sadeghipour, Forough, Faghihi, Mohammad Ali

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A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: a Case report por Ziyaee, Fateme, Shorafa, Eslam, Dastsooz, Hassan, Habibzadeh, Parham, Nemati, Hamid, Saeed, Amir, Silawi, Mohammad, Farazi Fard, Mohammad Ali, Faghihi, Mohammad Ali, Dastgheib, Seyed Alireza

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A Novel TTC19 Mutation in a Patient With Neurological, Psychological, and Gastrointestinal Impairment por Habibzadeh, Parham, Inaloo, Soroor, Silawi, Mohammad, Dastsooz, Hassan, Farazi Fard, Mohammad Ali, Sadeghipour, Forough, Faghihi, Zahra, Rezaeian, Mohaddeseh, Yavarian, Majid, Böhm, Johann, Faghihi, Mohammad Ali

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Genome-Wide Diversity, Population Structure and Demographic History of Dromedaries in the Central Desert of Iran por Bitaraf Sani, Morteza, Harofte, Javad Zare, Bitaraf, Ahmad, Esmaeilkhanian, Saeid, Banabazi, Mohammad Hossein, Salim, Nader, Teimoori, Abbas, Shafei Naderi, Ali, Faghihi, Mohammad Ali, Burger, Pamela Anna, Silawi, Mohammad, Taghipour Sheshdeh, Afsaneh

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Genomic prediction for growth using a low-density SNP panel in dromedary camels por Bitaraf Sani, Morteza, Zare Harofte, Javad, Banabazi, Mohammad Hossein, Esmaeilkhanian, Saeid, Shafei Naderi, Ali, Salim, Nader, Teimoori, Abbas, Bitaraf, Ahmad, Zadehrahmani, Mohammad, Burger, Pamela Anna, Landi, Vincenzo, Silawi, Mohammad, Taghipour Sheshdeh, Afsaneh, Faghihi, Mohammad Ali

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Expanding the molecular and clinical phenotypes of FUT8-CDG por Ng, Bobby G., Dastsooz, Hassan, Silawi, Mohammad, Habibzadeh, Parham, Jahan, Shima B., Fard, Mohammad A. F., Halliday, Benjamin J., Raymond, Kimiyo, Ruzhnikov, Maura R. Z., Tabatabaei, Zahra, Taghipour-Sheshdeh, Afsaneh, Brimble, Elise, Robertson, Stephen P., Faghihi, Mohammad A., Freeze, Hudson H.

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Identification of Candidate Genes for Pigmentation in Camels Using Genotyping-by-Sequencing por Bitaraf Sani, Morteza, Zare Harofte, Javad, Banabazi, Mohammad Hossein, Faraz, Asim, Esmaeilkhanian, Saeid, Naderi, Ali Shafei, Salim, Nader, Teimoori, Abbas, Bitaraf, Ahmad, Zadehrahmani, Mohammad, Burger, Pamela Anna, Asadzadeh, Nader, Silawi, Mohammad, Taghipour Sheshdeh, Afsaneh, Mohammad Nazari, Behrouz, Faghihi, Mohammad Ali, Roudbari, Zahra

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Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia por Farazi Fard, Mohammad Ali, Rebelo, Adriana P., Buglo, Elena, Nemati, Hamid, Dastsooz, Hassan, Gehweiler, Ina, Reich, Selina, Reichbauer, Jennifer, Quintáns, Beatriz, Ordóñez-Ugalde, Andrés, Cortese, Andrea, Courel, Steve, Abreu, Lisa, Powell, Eric, Danzi, Matt, Martuscelli, Nicole B., Bis-Brewer, Dana M., Tao, Feifei, Zarei, Fariba, Habibzadeh, Parham, Yavarian, Majid, Modarresi, Farzaneh, Silawi, Mohammad, Tabatabaei, Zahra, Yousefi, Masoume, Farpour, Hamid Reza, Kessler, Christoph, Mangold, Elisabeth, Kobeleva, Xenia, Mueller, Amelie J., Haack, Tobias B., Tarnopolsky, Mark, Gan-Or, Ziv, Rouleau, Guy A., Synofzik, Matthis, Sobrido, María-Jesús, Jordanova, Albena, Schüle, Rebecca, Zuchner, Stephan, Faghihi, Mohammad Ali

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Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia por Farazi Fard, Mohammad Ali, Rebelo, Adriana P., Buglo, Elena, Nemati, Hamid, Dastsooz, Hassan, Gehweiler, Ina, Reich, Selina, Reichbauer, Jennifer, Quintáns, Beatriz, Ordóñez-Ugalde, Andrés, Cortese, Andrea, Courel, Steve, Abreu, Lisa, Powell, Eric, Danzi, Matt C., Martuscelli, Nicole B., Bis-Brewer, Dana M., Tao, Feifei, Zarei, Fariba, Habibzadeh, Parham, Yavarian, Majid, Modarresi, Farzaneh, Silawi, Mohammad, Tabatabaei, Zahra, Yousefi, Masoume, Farpour, Hamid Reza, Kessler, Christoph, Mangold, Elisabeth, Kobeleva, Xenia, Tournev, Ivailo, Chamova, Teodora, Mueller, Amelie J., Haack, Tobias B., Tarnopolsky, Mark, Gan-Or, Ziv, Rouleau, Guy A., Synofzik, Matthis, Sobrido, María-Jesús, Jordanova, Albena, Schüle, Rebecca, Zuchner, Stephan, Faghihi, Mohammad Ali

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Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder por Polla, Daniel L., Fard, Mohammad Ali Farazi, Tabatabaei, Zahra, Habibzadeh, Parham, Levchenko, Olga A., Nikuei, Pooneh, Makrythanasis, Periklis, Hussain, Mureed, von Hardenberg, Sandra, Zeinali, Sirous, Fallah, Mohammad-Sadegh, Schuurs-Hoeijmakers, Janneke H. M., Shahzad, Mohsin, Fatima, Fareeha, Fatima, Neelam, Kaat, Laura Donker, Bruggenwirth, Hennie T., Fleming, Leah R., Condie, John, Ploski, Rafal, Pollak, Agnieszka, Pilch, Jacek, Demina, Nina A., Chukhrova, Alena L., Sergeeva, Vasilina S., Venselaar, Hanka, Masri, Amira T., Hamamy, Hanan, Santoni, Federico A., Linda, Katrin, Ahmed, Zubair M., Kasri, Nael Nadif, de Brouwer, Arjan P. M., Bergmann, Anke K., Hethey, Sven, Yavarian, Majid, Ansar, Muhammad, Riazuddin, Saima, Riazuddin, Sheikh, Silawi, Mohammad, Ruggeri, Gaia, Pirozzi, Filomena, Eftekhar, Ebrahim, Sheshdeh, Afsaneh Taghipour, Bahramjahan, Shima, Mirzaa, Ghayda M., Lavrov, Alexander V., Antonarakis, Stylianos E., Faghihi, Mohammad Ali, van Bokhoven, Hans

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