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/vufind/Search/Results?lookfor=%22Mehvari%2C+Sepideh%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Mehvari%2C+Sepideh%22&type=Person&sort=year
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PubPharm (8)
1
Contribution of genetic variants in the development of familial premature coronary artery disease in a cohort of cardiac patients
enthalten in:
Clinical genetics
| 2024
von
Mehvari, S.
|
Karimian Fathi, N.
|
Saki, S.
| +18
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2
Contribution of genetic variants in the development of familial premature coronary artery disease in a cohort of cardiac patients
enthalten in:
Clinical Genetics
| 2024
von
Mehvari, S.
|
Karimian Fathi, N.
|
Saki, S.
| +18
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3
Comprehensive genotype-phenotype correlation in AP-4 deficiency syndrome; Adding data from a large cohort of Iranian patients
enthalten in:
Clinical genetics
| 2021
von
Beheshtian, M.
|
Akhtarkhavari, T.
|
Mehvari, S.
| +12
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4
Whole genome sequencing identifies a duplicated region encompassing Xq13.2q13.3 in a large Iranian family with intellectual disability
enthalten in:
Molecular genetics & genomic medicine
| 2020
von
Mehvari, S.
|
Larti, F.
|
Hu, H.
| +10
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5
Whole genome sequencing identifies a duplicated region encompassing Xq13.2q13.3 in a large Iranian family with intellectual disability
enthalten in:
Molecular Genetics & Genomic Medicine
| 2020
von
Mehvari, S.
|
Larti, F.
|
Hu, H.
| +10
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6
Genetics of intellectual disability in consanguineous families
enthalten in:
Molecular psychiatry
| 2019
von
Hu, H.
|
Kahrizi, K.
|
Musante, L.
| +49
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7
Effect of inbreeding on intellectual disability revisited by trio sequencing
enthalten in:
Clinical genetics
| 2019
von
Kahrizi, K.
|
Hu, H.
|
Hosseini, M.
| +28
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8
Effect of inbreeding on intellectual disability revisited by trio sequencing
enthalten in:
Clinical Genetics
| 2019
von
Kahrizi, K.
|
Hu, H.
|
Hosseini, M.
| +28
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Clinical genetics
2
Clinical Genetics
1
Molecular Genetics & Genomic Medicine
1
Molecular genetics & genomic medicine
1
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5
Journal Article
5
Research Support, Non-U.S. Gov't
2
intellectual disability
1
AP-4 deficiency syndrome
1
Adaptor Protein Complex 4
1
Case Reports
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EC 2.3.2.27
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Iranian families
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Monocarboxylic Acid Transporters
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NEXMIF protein, human
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Nerve Tissue Proteins
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RLIM protein, human
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SLC16A2 protein, human
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Ubiquitin-Protein Ligases
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Xq duplication
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Xq13.2q13.3
1
atherosclerosis
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consanguinity
1
coronary artery disease
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2020-
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2010-2019
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