檢索結果 - Fattahi, Zohreh

Novel variants in Iranian individuals suspected to have inherited red blood cell disorders, including bone marrow failure syndromes 由 Neishabury, Maryam, Mehri, Maghsood, Fattahi, Zohreh, Najmabadi, Hossein, Azarkeivan, Azita

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Did the GJB2 35delG Mutation Originate in Iran? 由 Norouzi, Vahideh, Azizi, Hiva, Esteghamat, Fatemehsadat, Bazazzadegan, Niloofar, Fattahi, Zohreh, Nishimura, Carla, Nikzat, Nooshin, Jalalvand, Khadijeh, Kahrizi, Kimia, Smith, Richard. J. H., Najmabadi, Hossein

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The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families 由 Davarniya, Behzad, Hu, Hao, Kahrizi, Kimia, Musante, Luciana, Fattahi, Zohreh, Hosseini, Masoumeh, Maqsoud, Fariba, Farajollahi, Reza, Wienker, Thomas F., Ropers, H. Hilger, Najmabadi, Hossein

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Whole genome sequencing identifies a duplicated region encompassing Xq13.2q13.3 in a large Iranian family with intellectual disability 由 Mehvari, Sepideh, Larti, Farzaneh, Hu, Hao, Fattahi, Zohreh, Beheshtian, Maryam, Abedini, Seyedeh Sedigheh, Arzhangi, Sanaz, Ropers, Hans‐Hilger, Kalscheuer, Vera M., Auld, Daniel, Kahrizi, Kimia, Riazalhosseini, Yasser, Najmabadi, Hossein

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Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation 由 Hildebrand, Michael S., Thorne, Natalie P., Bromhead, Catherine J., Kahrizi, Kimia, Webster, Jennifer A., Fattahi, Zohreh, Bataejad, Mojgan, Kimberling, William J., Stephan, Dietrich, Najmabadi, Hossein, Bahlo, Melanie, Smith, Richard J.H.

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A defect in the CLIP1 gene (CLIP-170) can cause autosomal recessive intellectual disability 由 Larti, Farzaneh, Kahrizi, Kimia, Musante, Luciana, Hu, Hao, Papari, Elahe, Fattahi, Zohreh, Bazazzadegan, Niloofar, Liu, Zhe, Banan, Mehdi, Garshasbi, Masoud, Wienker, Thomas F, Ropers, H Hilger, Galjart, Niels, Najmabadi, Hossein

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A defect in the CLIP1 gene (CLIP-170) can cause autosomal recessive intellectual disability 由 Larti, Farzaneh, Kahrizi, Kimia, Musante, Luciana, Hu, Hao, Papari, Elahe, Fattahi, Zohreh, Bazazzadegan, Niloofar, Liu, Zhe, Banan, Mehdi, Garshasbi, Masoud, Wienker, Thomas F, Hilger Ropers, H, Galjart, Niels, Najmabadi, Hossein

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Screening for MYO15A Gene Mutations in Autosomal Recessive Nonsyndromic, GJB2 Negative Iranian Deaf Population 由 Fattahi, Zohreh, Shearer, A. Eliot, Babanejad, Mojgan, Bazazzadegan, Niloofar, Almadani, Seyed Navid, Nikzat, Nooshin, Jalalvand, Khadijeh, Arzhangi, Sanaz, Esteghamat, Fatemehsadat, Abtahi, Rezvan, Azadeh, Batool, Smith, Richard J.H., Kahrizi, Kimia, Najmabadi, Hossein

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Brief Report of Variants Detected in Hereditary Hearing Loss Cases in Iran over a 3-Year Period 由 BAZAZZADEGAN, Niloofar, VAZEHAN, Raheleh, FADAEE, Mahsa, FATTAHI, Zohreh, ABOLHASSANI, Ayda, PARSIMEHR, Elham, KALHOR, Zahra, FARAJI ZONOOZ, Mehrshid, AHANGARI, Fatemeh, DEHDAHSI, Shima, SAMIEE, Farshide, JAMALI, Payman, HABIBI, Haleh, NOURIZADEH, Younes, MAHDAVI, Shokouh, BEHESHTIAN, Maryam, KARIMINEJAD, Ariana, SMITH, Richard JH, NAJMABADI, Hossein

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Biallelic mutations in the death domain of PIDD1 impair caspase-2 activation and are associated with intellectual disability 由 Sheikh, Taimoor I., Vasli, Nasim, Pastore, Stephen, Kharizi, Kimia, Harripaul, Ricardo, Fattahi, Zohreh, Pande, Shruti, Naeem, Farooq, Hussain, Abrar, Mir, Asif, Islam, Omar, Girisha, Katta Mohan, Irfan, Muhammad, Ayub, Muhammad, Schwarzer, Christoph, Najmabadi, Hossein, Shukla, Anju, Sladky, Valentina C., Braun, Vincent Zoran, Garcia-Carpio, Irmina, Villunger, Andreas, Vincent, John B.

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ZBTB11 dysfunction: spectrum of brain abnormalities, biochemical signature and cellular consequences 由 Sumathipala, Dulika, Strømme, Petter, Fattahi, Zohreh, Lüders, Torben, Sheng, Ying, Kahrizi, Kimia, Einarsen, Ingunn Holm, Sloan, Jennifer L, Najmabadi, Hossein, van den Heuvel, Lambert, Wevers, Ron A, Guerrero-Castillo, Sergio, Mørkrid, Lars, Valayannopoulos, Vassili, Backe, Paul Hoff, Venditti, Charles P, van Karnebeek, Clara D, Nilsen, Hilde, Frengen, Eirik, Misceo, Doriana

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Distinct genetic variation and heterogeneity of the Iranian population 由 Mehrjoo, Zohreh, Fattahi, Zohreh, Beheshtian, Maryam, Mohseni, Marzieh, Poustchi, Hossein, Ardalani, Fariba, Jalalvand, Khadijeh, Arzhangi, Sanaz, Mohammadi, Zahra, Khoshbakht, Shahrouz, Najafi, Farid, Nikuei, Pooneh, Haddadi, Mohammad, Zohrehvand, Elham, Oladnabi, Morteza, Mohammadzadeh, Akbar, Jafari, Mandana Hadi, Akhtarkhavari, Tara, Gooshki, Ehsan Shamsi, Haghdoost, Aliakbar, Najafipour, Reza, Niestroj, Lisa-Marie, Helwing, Barbara, Gossmann, Yasmina, Toliat, Mohammad Reza, Malekzadeh, Reza, Nürnberg, Peter, Kahrizi, Kimia, Najmabadi, Hossein, Nothnagel, Michael

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SARS‐CoV‐2 outbreak in Iran: The dynamics of the epidemic and evidence on two independent introductions 由 Fattahi, Zohreh, Mohseni, Marzieh, Jalalvand, Khadijeh, Aghakhani Moghadam, Fatemeh, Ghaziasadi, Azam, Keshavarzi, Fatemeh, Yavarian, Jila, Jafarpour, Ali, Mortazavi, Seyedeh Elham, Ghodratpour, Fatemeh, Behravan, Hanieh, Khazeni, Mohammad, Momeni, Seyed Amir, Jahanzad, Issa, Moradi, Abdolvahab, Tabarraei, Alijan, Azimi, Sadegh Ali, Kord, Ebrahim, Hashemi‐Shahri, Seyed Mohammad, Azaran, Azarakhsh, Yousefi, Farid, Mokhames, Zakiye, Soleimani, Alireza, Ghafari, Shokouh, Ziaee, Masood, Habibzadeh, Shahram, Jeddi, Farhad, Hadadi, Azar, Abdollahi, Alireza, Kaydani, Gholam Abbas, Soltani, Saber, Mokhtari‐Azad, Talat, Najafipour, Reza, Malekzadeh, Reza, Kahrizi, Kimia, Jazayeri, Seyed Mohammad, Najmabadi, Hossein

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