Resultados da busca - Fattahi, Zohreh

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

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Did the GJB2 35delG Mutation Originate in Iran? por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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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