Paynantheine more effectively reverses multidrug resistance in malignant EPG85.257RDB and MCF7MX cells than morphine and speciociliatine von Abdali, Nayereh, Nadipour Borujeni, Mohammad, Hosseini, Sayedeh Azimeh, Malekzadeh, Rahim, Abolhasani, Marzieh, Mirzaei, Seyed Abbas, Elahian, Fatemeh

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The associations between lying with Physical and Mental health statute students at University of Shahrekord, Iran von Dehkordi, Mansoureh Kiani, Astaneh, Ali Nazeri, Abdali, Nayereh, Kiani, Freshteh, Madmoli, Mostafa, Khaledi, Mansoor, Lotfizadeh, Masoud

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Non-syndromic cleft palate: Association analysis on three gene polymorphisms of the folate pathway in Asian and Italian populations von Carinci, Francesco, Palmieri, Annalisa, Scapoli, Luca, Cura, Francesca, Borelli, Francesco, Morselli, Paolo Giovanni, Nouri, Nayereh, Abdali, Hossein, Gianni, Aldo Bruno, Russillo, Antonio, Docimo, Raffaella, Martinelli, Marcella

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Reciprocal 22q11.2 Deletion and Duplication in Siblings with Karyotypically Normal Parents von Demaerel, Wolfram, Hosseinzadeh, Majid, Nouri, Nayereh, Sedghi, Maryam, Dimitriadou, Eftychia, Salehi, Mansoor, Abdali, Hossein, Memarzadeh, Mehrdad, Zamani, Mahdi, Vermeesch, Joris

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Reciprocal 22q11.2 Deletion and Duplication in Siblings with Karyotypically Normal Parents von Demaerel, Wolfram, Hosseinzadeh, Majid, Nouri, Nayereh, Sedghi, Maryam, Dimitriadou, Eftychia, Salehi, Mansoor, Abdali, Hossein, Memarzadeh, Mehrdad, Zamani, Mahdi, Vermeesch, Joris R.

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A case report of 22q11 deletion syndrome confirmed by array-CGH method von Sedghi, Maryam, Nouri, Narges, Abdali, Hossein, Memarzadeh, Mehrdad, Nouri, Nayereh

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Prevalence of 22q11.2 microdeletion syndrome in Iranian patients with cleft palate von Nouri, Narges, Memarzadeh, Mehrdad, Salehi, Mansoor, Nouri, Nayereh, Meamar, Rokhsareh, Behnam, Mahdiyeh, Derakhshandeh, Fatemeh, Kashkoolinejad, Tahereh, Abdali, Hossein

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Identification of Proximal and Distal 22q11.2 Microduplications among Patients with Cleft Lip and/or Palate: A Novel Inherited Atypical 0.6Mb Duplication von Maryam Sedghi, Hossein Abdali, Mehrdad Memarzadeh, Mansoor Salehi, Narges Nouri, Majid Hosseinzadeh, Nayereh Nouri

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Identification of Proximal and Distal 22q11.2 Microduplications among Patients with Cleft Lip and/or Palate: A Novel Inherited Atypical 0.6 Mb Duplication von Sedghi, Maryam, Abdali, Hossein, Memarzadeh, Mehrdad, Salehi, Mansoor, Nouri, Narges, Hosseinzadeh, Majid, Nouri, Nayereh

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Investigation of TBX1 gene deletion in Iranian children with 22q11.2 deletion syndrome: correlation with conotruncal heart defects: Table 1 von Ganji, Hamid, Salehi, Mansoor, Sedghi, Maryam, Abdali, Hossein, Nouri, Nayereh, Sadri, Leyli, Hosseinzadeh, Majid, Vakili, Bahareh, Lotfi, Mahdi

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Investigation of TBX1 gene deletion in Iranian children with 22q11.2 deletion syndrome: correlation with conotruncal heart defects von Ganji, Hamid, Salehi, Mansoor, Sedghi, Maryam, Abdali, Hossein, Nouri, Nayereh, Sadri, Leyli, Hosseinzadeh, Majid, Vakili, Bahareh, Lotfi, Mahdi

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A case report of 22q11 deletion syndrome confirmed by array-CGH method von Sedghi, Maryam, Nouri, Narges, Abdali, Hossein, Memarzadeh, Mehrdad, Nouri, Nayereh

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