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1دورية أكاديمية
المؤلفون: Ayda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, Mahsa Fadaee, Raheleh Vazehan, Fatemeh Ahangari, Shima Dehdahsi, Mehrshid Faraji Zonooz, Elham Parsimehr, Zahra Kalhor, Fatemeh Peymani, Maryam Mozaffarpour Nouri, Mojgan Babanejad, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Fariba Afroozan, Hilda Yazdan, Bita Bozorgmehr, Azita Azarkeivan, Shokouh Sadat Mahdavi, Pooneh Nikuei, Farzad Fatehi, Payman Jamali, Mahmoud Reza Ashrafi, Parvaneh Karimzadeh, Haleh Habibi, Kimia Kahrizi, Shahriar Nafissi, Ariana Kariminejad, Hossein Najmabadi
المصدر: npj Genomic Medicine, Vol 9, Iss 1, Pp 1-11 (2024)
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2056-7944
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2دورية أكاديمية
المؤلفون: Ayda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, Mahsa Fadaee, Raheleh Vazehan, Fatemeh Ahangari, Shima Dehdahsi, Mehrshid Faraji Zonooz, Elham Parsimehr, Zahra Kalhor, Fatemeh Peymani, Maryam Mozaffarpour Nouri, Mojgan Babanejad, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Fariba Afroozan, Hilda Yazdan, Bita Bozorgmehr, Azita Azarkeivan, Shokouh Sadat Mahdavi, Pooneh Nikuei, Farzad Fatehi, Payman Jamali, Mahmoud Reza Ashrafi, Parvaneh Karimzadeh, Haleh Habibi, Kimia Kahrizi, Shahriar Nafissi, Ariana Kariminejad, Hossein Najmabadi
المصدر: Genetics in Medicine Open, Vol 2, Iss , Pp 101510- (2024)
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Fereshteh Jamshidi, Ebrahim Shokouhian, Marzieh Mohseni, Kimia Kahrizi, Hossein Najmabadi, Mojgan Babanejad
المصدر: Molecular Genetics & Genomic Medicine, Vol 11, Iss 5, Pp n/a-n/a (2023)
مصطلحات موضوعية: FGF3, Iran, LAMM syndrome, whole‐exome sequencing, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2324-9269
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4دورية أكاديمية
المؤلفون: Kimia Najafi, Soheila Gholami, Azadeh Moshtagh, Masood Bazrgar, Neda Sadatian, Golemaryam Abbasi, Parvin Rostami, Soheila Khalili, Mojgan Babanejad, Bahareh Nourmohammadi, Negin Faramarzi Garous, Hossein Najmabadi, Roxana Kariminejad
المصدر: Molecular Genetics & Genomic Medicine, Vol 7, Iss 8, Pp n/a-n/a (2019)
مصطلحات موضوعية: array comparative genomic hybridization, chromosomal abnormality, consanguinity, miscarriage, recurrent abortion, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2324-9269
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5دورية أكاديمية
المؤلفون: Reyhaneh Kameli, Mandana Hasanzad, Zahra Tahmasebi Fard, Mojgan Babanejad, Mahdieh Imeni, Lotfollah Feizi Barnaji, Atoosa Madadkar, Seyed Hamid Jamaldini
المصدر: Research in Molecular Medicine, Vol 4, Iss 4, Pp 38-44 (2016)
وصف الملف: electronic resource
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6دورية أكاديمية
المؤلفون: Reihaneh Alikhani, Fatemeh Ostaresh, Mojgan Babanejad, Nilofar Bazazzadegan, Hossein Najmabadi, Kimia Kahrizi
المصدر: Iranian Rehabilitation Journal, Vol 13, Iss 3, Pp 64-68 (2015)
مصطلحات موضوعية: Autosomal recessive non-syndromic hearing loss, Homozygosity mapping, Linkage analysis, Iran, Medicine, Vocational rehabilitation. Employment of people with disabilities, HD7255-7256
وصف الملف: electronic resource
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7دورية أكاديمية
المؤلفون: Mahdieh Imeni, Mandana Hasanzad, Tahereh Naji, Behzad Poopak, Mojgan Babanejad, Hamid Reza Sanati, Reyhaneh Kameli, Atoosa Madadkar, Zahra Hosseini Khah, Seyed Hamid Jamaldini
المصدر: Research in Molecular Medicine, Vol 1, Iss 3, Pp 18-23 (2013)
مصطلحات موضوعية: Coronary artery disease (CAD), Lipoprotein lipase (LPL), Hind III Polymorphism, RFLP, dyslipidemia, Medicine (General), R5-920
وصف الملف: electronic resource
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8دورية أكاديمية
المؤلفون: Seyed Hamid Jamaldini, Mojgan Babanejad, Reza Mozaffari, Nooshin Nikzat, Khadijeh Jalalvand, Azadeh Badiei, Hamidreza Sanati, Farshad Shakerian, Mahdi Afshari, Kimia Kahrizi, Hossein Najmabadi
المصدر: Acta Medica Iranica, Vol 52, Iss 5 (2014)
مصطلحات موضوعية: Coronary artery disease, LDLR locus, Single nucleotide polymorphism, SMARCA4 gene, Medicine (General), R5-920
وصف الملف: electronic resource
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9
المؤلفون: Mojgan Babanejad, Maryam Beheshtian, Fereshteh Jamshidi, Marzieh Mohseni, Kevin T. Booth, Kimia Kahrizi, Hossein Najmabadi
المصدر: Human Genetics. 141:623-631
مصطلحات موضوعية: Hearing Loss, Sensorineural, Mutation, Genetics, Humans, Deafness, Iran, Hearing Loss, Genetics (clinical), Pedigree
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10
المؤلفون: Kimia Kahrizi, Fariba Ardalani, Mojdeh Akbari, Mojgan Babanejad, Kevin T. Booth, Hossein Najmabadi, Haleh Habibi, Khadijeh Jalalvand, Nooshin Nikzat, Fatemeh Ghodratpour, Omid Ali Adeli, Marzieh Mohseni, Payman Jamali, Hela Azaiez, Sanaz Arzhangi
المصدر: J Hum Genet
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Proband, Adolescent, Genotype, Hearing loss, Hearing Loss, Sensorineural, Iran, 030105 genetics & heredity, Biology, Article, Frameshift mutation, Male infertility, Diagnosis, Differential, Young Adult, 03 medical and health sciences, Exon, Genetics, medicine, Humans, Genetic Predisposition to Disease, Frameshift Mutation, Hearing Loss, Gene, Genetic Association Studies, Infertility, Male, Genetics (clinical), Loss function, High-Throughput Nucleotide Sequencing, Exons, medicine.disease, Pedigree, 030104 developmental biology, Mutation (genetic algorithm), Female, Protein Tyrosine Phosphatases, medicine.symptom