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فیلتر نتایج
نتایج 11 تا 20 از مجموع 20
1
2
Journal Paper
Retinitis pigmentosa: A Case Report with Thr۱۷Arg as a Novel Mutation in RHO Gene.
Authors:
sajjad; Rafiee Komachali
،
Zakieh Siahpoosh
،
Mansoor Salehi
Year 1401
Publish place:
Journal of Epigenetics Issue 1، Vol 3
Pages:
6
| Language: English
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Journal Paper
Identification of a Novel CLCNKB Mutation in an Iranian Family with Bartter Syndrome Type ۳.
Authors:
Javad Mohammadi-asl
،
Heshmatolah Shahbazian
،
Farzad Jasemi Zergani
،
Alireza Kheradmand
Year 1400
Publish place:
Journal of Advances in Medical and Biomedical Research Issue 139، Vol 30
Pages:
5
| Language: English
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Journal Paper
PLA۲G۶ gene mutation and infantile neuroaxonal degeneration; report of three cases from Iran
Authors:
Reza Jafarzadeh Esfehani
،
Atieh Eslahi
،
Mehran Beiraghi Toosi
،
Ariane Sadrnabavi
،
Mohammad Amin Kerachian
،
Mahsa Sadat Mohajeri Asl
،
Mahsa Farjami
،
Farzaneh Alizadeh
،
Majid Mojarad
Year 1400
Publish place:
Iranian Journal of Basic Medical Sciences Issue 9، Vol 24
Pages:
6
| Language: English
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Journal Paper
Whole-Exome Sequencing Identified a Novel Variant (C.۴۰۵_۴۲۲+۳۹del) in DSP Gene in an Iranian Pedigree with Familial Dilated Cardiomyopathy
Authors:
Yeganeh Eshaghkhani
،
Arezoo Mohamadifar
،
Mostafa Asadollahi
،
Mahdieh Taghizadeh
،
Arezou Karamzade
،
Mohammad Saberi
،
Parisa Nourmohammadi
،
Zahra Golchehre
،
Ahmad Amin
،
Mohammad Keramatipour
Year 1400
Publish place:
Reports of Biochemistry and Molecular Biology Issue 2، Vol 10
Pages:
8
| Language: English
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Journal Paper
Identification of the Peroxisomal Biogenesis Factor ۱ Gene Point Mutation in an Iranian Family with Zellweger Syndrome (ZS)
Authors:
Negin Parsamanesh
،
Aazam Ahmadi Shadmehri
،
Shahnaz Zarifi
،
Ebrahim Miri-Moghaddam
Year 1400
Publish place:
Journal of Advances in Medical and Biomedical Research Issue 134، Vol 29
Pages:
9
| Language: English
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Journal Paper
مروری بر علل ژنتیکی آستنوزوسپرمی
Authors:
اروند اکبری
،
زهرا انوار
،
مجتبی جعفری نیا
،
مهدی توتونچی
Year 1398
Publish place:
Journal of Kashan University of Medical Sciences Issue 3، Vol 23
Pages:
16
| Language: Persian
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Journal Paper
Strategies for whole-exome sequencing analysis in a case series study of familial male infertility
Authors:
Masomeh Askari
،
Dor Mohammad Kordi Tamandani
،
Navid almadani
،
Mehdi Totonchi
Year 1399
Publish place:
International Journal of Reproductive BioMedicine Issue 5، Vol 18
Pages:
10
| Language: English
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Journal Paper
Strategies and Clinical Applications of Next Generation Sequencing
Authors:
Shohreh Khorshidi
،
Alireza Palangi
Year 1397
Publish place:
Multidisciplinary Cancer Investigation Issue 4، Vol 2
Pages:
11
| Language: English
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Journal Paper
Identification of a novel homozygous mutation in the DDR2 gene from a patient with spondylo-meta-epiphyseal dysplasia by whole exome sequencing
Authors:
Masoud Heidari
،
Morteza Soleyman-Nejad
،
Alireza Isazadeh
،
Mohammad Hossein Taskiri
،
Manzar Bolhassani
،
Nahid Sadighi
،
Zahra Shiri
،
Zahra Karimi
،
Mansour Heidari
Year 1400
Publish place:
Iranian Journal of Basic Medical Sciences Issue 2، Vol 24
Pages:
5
| Language: English
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Journal Paper
Whole exome sequencing revealed a novel dystrophin-related protein-2 (DRP2) deletion in an Iranian family with symptoms of polyneuropathy
Authors:
Maryam Tahmasebi Birgani
،
Mohammadreza Hajjari
،
Neda Golchin
،
Bita Shalbafan
Year 1398
Publish place:
Iranian Journal of Basic Medical Sciences Issue 5، Vol 22
Pages:
5
| Language: English
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نتایج 11 تا 20 از مجموع 20
1
2