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Tabatabaiefar, Mohammad Amin
159  results:
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1

Clinical characterizations and molecular genetic study of t..:

Nouri, Zahra ; Sarmadi, Akram ; Narrei, Sina...
BMC Medical Genomics.  17 (2024)  1 - p. , 2024
Link: https://doi.org/10.1186/..
 
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2

Monogenic etiologies of persistent human papillomavirus inf..:

Biglari, Sajjad ; Moghaddam, Atefeh Sohanforooshan ; Tabatabaiefar, Mohammad Amin...
Genetics in Medicine.  26 (2024)  2 - p. 101028 , 2024
Link: https://doi.org/10.1016/..
 
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3

RARS1‐related hypomyelinating leukodystrophy‐9 (HLD‐9) in t..:

Biglari, Sajjad ; Vahidnezhad, Hassan ; Tabatabaiefar, Mohammad Amin..
Molecular Genetics & Genomic Medicine.  12 (2024)  4 - p. , 2024
Link: https://doi.org/10.1002/..
 
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4

Decellularized skin pretreatment by monophosphoryl lipid A ..:

Jalili, Ali ; Shojaei-Ghahrizjani, Fereshteh ; Tabatabaiefar, Mohammad Amin.
Molecular Biology Reports.  51 (2024)  1 - p. , 2024
Link: https://doi.org/10.1007/..
 
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5

A novel METTL5 variant disrupting a donor splice site leads..:

Shakarami, Fatemeh ; Nouri, Zahra ; Khanahmad, Hossein..
Journal of Genetics.  102 (2023)  2 - p. , 2023
Link: https://doi.org/10.1007/..
 
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6

Molecular and phenotypical findings of a novel de novo SYNG..:

Mir, Atefeh ; Song, Yongjun ; Lee, Hane...
Laboratory Medicine.  55 (2023)  2 - p. 204-208 , 2023
Link: https://doi.org/10.1093/..
 
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7

A novel heterozygous truncating variant in the AGO1 gene in..:

Mir, Atefeh ; Khorram, Erfan ; Song, Yongjun..
Annals of Human Genetics.  87 (2023)  6 - p. 295-301 , 2023
Link: https://doi.org/10.1111/..
 
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8

Familial nonmedullary thyroid cancer: a case series in Iran..:

Mohammadi Zaniani, Zohreh ; Zeinalian, Mehrdad ; Tabatabaiefar, Mohammad Amin
Laboratory Medicine.  55 (2023)  4 - p. 506-516 , 2023
Link: https://doi.org/10.1093/..
 
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9

Whole exome sequencing revealed variants in four genes unde..:

Mir, Atefeh ; Song, Yongjun ; Lee, Hane...
BMC Medical Genomics.  16 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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10

Novel in-frame duplication variant characterization in late..:

Ataei, Zahra ; Nouri, Zahra ; Tavakoli, Farial...
PLOS ONE.  18 (2023)  2 - p. e0282304 , 2023
Link: https://doi.org/10.1371/..
 
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11

A novel de novo frameshift variant in the CHD2 gene related..:

Mir, Atefeh ; Song, Yongjun ; Lee, Hane..
Molecular Genetics & Genomic Medicine.  12 (2023)  1 - p. , 2023
Link: https://doi.org/10.1002/..
 
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12

A deleterious frameshift insertion mutation in the ZNF142 g..:

Mir, Atefeh ; Song, Yongjun ; Lee, Hane...
Molecular Genetics & Genomic Medicine.  11 (2023)  12 - p. , 2023
Link: https://doi.org/10.1002/..
 
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13

New molecular insights into the A218V variant impact on the..:

Aghaei, Shahrzad ; Farrokhi, Effat ; saffari-chaleshtori, Javad...
Molecular Genetics and Genomics.  298 (2023)  3 - p. 693-708 , 2023
Link: https://doi.org/10.1007/..
 
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14

Griscelli syndrome type 1: a novel pathogenic variant, and ..:

Khorram, Erfan ; Tabatabaiefar, Mohammad Amin ; Yaghini, Omid...
Molecular Genetics and Genomics.  298 (2023)  2 - p. 485-493 , 2023
Link: https://doi.org/10.1007/..
 
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15

X‐linked mental retardation‐hypotonic facies syndrome: Exom..:

Shakarami, Fatemeh ; Jahani, Mehdi ; Nouri, Zahra.
Molecular Genetics & Genomic Medicine.  10 (2022)  10 - p. , 2022
Link: https://doi.org/10.1002/..
 
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