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فیلتر نتایج
MohammadMehdi Heidari
Journal Paper
A Splicing Variant in OCRL Gene Might Explain the Second Case of Lowe Syndrome in Iran
Authors:
Massoud Houshmand
،
Gholamreza Babamohammadi
،
Hamidreza Moazzeni
،
Ahmad Reza Salehi Chaleshtori
،
Mohammad Taghi Akbari
Year 1397
Publish place:
Human Genetics and Genomics Issue 1، Vol 3
Pages:
7
| Language: English
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Journal Paper
Personal Medicine Possible Treatment of Breast Cancer
Authors:
Fateme Davodabadi
،
Massoud Houshmand
Year 1400
Publish place:
Personalized Medicine Journal Issue 23، Vol 6
Pages:
7
| Language: English
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Journal Paper
The Role of Mitochondria in The Development and Progression of Cancer
Authors:
Fateme Davodabadi
،
Massoud Houshmand
Year 1400
Publish place:
Personalized Medicine Journal Issue 22، Vol 6
Pages:
7
| Language: English
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Journal Paper
The mitochondrial DNA mutations associated with cardiac arrhythmia investigated in an LQTS family
Authors:
Fatemeh Khatami
،
Mohammad Mehdi Heidari
،
Massoud Houshmand
Year 1393
Publish place:
Iranian Journal of Basic Medical Sciences Issue 9، Vol 17
Pages:
6
| Language: English
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Journal Paper
Profile of Iranian GJB۲ Mutations in Young Population with Novel Mutation
Authors:
Masoumeh Falah
،
Massoud Houshmand
،
Susan Akbaroghli
،
Saeid Mahmodian
،
Yaser Ghavami
،
Mohammad Farhadi
Year 1390
Publish place:
Iranian Journal of Basic Medical Sciences Issue 3، Vol 14
Pages:
6
| Language: English
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Journal Paper
Association of mtDNA mutation with Autism in Iranian patients
Authors:
Massoud Houshmand
،
Kazem Mousavizadeh
،
Mohammad Askari
،
Amin Reza Nikpour
Year 1392
Publish place:
International Journal of Pediatrics Issue 1، Vol 1
Pages:
5
| Language: English
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Journal Paper
The point mutations of mitochondrial tRNA threonine and proline in idiopathic repeated pregnancy loss
Authors:
Seyed Mohammad Seyedhassani
،
Massoud Houshmand
،
Seyed Mehdi Kalantar
،
Abbas Aflatoonian
Year 1389
Publish place:
International Journal of Reproductive BioMedicine Issue 1، Vol 8
Pages:
6
| Language: English
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Conference Paper
Mitochondrial Disorders and Diagnosis
Authors:
Massoud Houshmand
Year 1384
Publish place:
04th National Biotechnology Congress of Iran
Pages:
5
| Language: English
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Conference Paper
Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations, haplogroup association and mitochondrial deletions in Iranian patients with Friedreich's Ataxia
Authors:
Mehdi Shafa Shariat Panahi
،
Massoud Houshmand
،
Mohammad Hossein Sanati
،
Shahriar Nafisi
Year 1384
Publish place:
04th National Biotechnology Congress of Iran
Pages:
10
| Language: English
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Conference Paper
Haplogroup distribution and Polymorphism in the non-coding region of human Mitochondrial DNA in patients harboring the primary G11778A, G3460A, T14484C mutations
Authors:
Massoud Houshmand
،
Mehdi Shafa Shariat Panahi
،
Abdol Reza Tabassi
،
Mohammad Hossein Sanati
Year 1384
Publish place:
04th National Biotechnology Congress of Iran
Pages:
10
| Language: English
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