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Fatemeh Bitarafan
50
results:
Search for persons
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Format
Online (50)
Mediatypes
Articles (Online) (19)
Bookchapter (Online) (2)
OpenAccess-fulltext (29)
Languages
english (46)
Sorted by: Relevance
Sorted by: Year
?
1
Homozygous TREM2 c.549del; p.(Leu184Serfs*5) variant causin..:
Gilani, Naser
;
Bitarafan, Fatemeh
;
Ozaslan, Mehmet
...
Molecular Genetics & Genomic Medicine. 12 (2024) 6 - p. , 2024
Link:
https://doi.org/10.1002/..
?
2
Biallelic NDUFA4 Deletion Causes Mitochondrial Complex IV D..:
Misceo, Doriana
;
Strømme, Petter
;
Bitarafan, Fatemeh
...
Genes. 15 (2024) 4 - p. 500 , 2024
Link:
https://doi.org/10.3390/..
?
3
A biallelic variant in POLR2C is associated with congenital..:
Bitarafan, Fatemeh
;
Razmara, Ehsan
;
Jafarinia, Ehsan
..
European Journal of Clinical Investigation. 53 (2023) 4 - p. , 2023
Link:
https://doi.org/10.1111/..
?
4
Expanding phenotype heterogeneity of NARS2 by presenting su..:
Khodaeian, Mehrnoosh
;
Bitarafan, Fatemeh
;
Garrousi, Fatemeh
...
Journal of Clinical Laboratory Analysis. 37 (2023) 21-22 - p. , 2023
Link:
https://doi.org/10.1002/..
?
5
Reporting a novel growth hormone receptor gene variant in a..:
Bitarafan, Fatemeh
;
Khodaeian, Mehrnoosh
;
Garrousi, Fatemeh
...
BMC Endocrine Disorders. 23 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
6
Identification of GJB2 Variants in 75 Unrelated Iranian Aut..:
Bitarafan, Fatemeh
;
Seyedena, Seyed Yousef
;
Mahmoudi, Mahdi
.
Journal of Human Genetics and Genomics. 4 (2022) 1 - p. , 2022
Link:
https://doi.org/10.5812/..
?
7
Prevalence and Genotype Distribution of Human Papillomaviru..:
Bitarafan, Fatemeh
;
Hekmat, Mohammad Reza
;
Khodaeian, Mehrnoosh
...
International Journal of Infectious Diseases. 111 (2021) - p. 295-302 , 2021
Link:
https://doi.org/10.1016/..
?
8
Identification of a novel MICU1 nonsense variant causes myo..:
Bitarafan, Fatemeh
;
Khodaeian, Mehrnoosh
;
Amjadi Sardehaei, Elham
...
Molecular and Cellular Pediatrics. 8 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1186/..
?
9
Novel homozygous variants in the TMC1 and CDH23 genes cause..:
Zardadi, Safoura
;
Razmara, Ehsan
;
Asgaritarghi, Golareh
...
Molecular Genetics & Genomic Medicine. 8 (2020) 12 - p. , 2020
Link:
https://doi.org/10.1002/..
?
10
Three Novel Variants identified in FBN1 and TGFBR2 in seven..:
Bitarafan, Fatemeh
;
Razmara, Ehsan
;
Khodaeian, Mehrnoosh
...
Molecular Genetics & Genomic Medicine. 8 (2020) 8 - p. , 2020
Link:
https://doi.org/10.1002/..
?
11
A homozygote variant in the tRNA splicing endonuclease subu..:
Sepahvand, Afrooz
;
Razmara, Ehsan
;
Bitarafan, Fatemeh
...
Molecular Genetics & Genomic Medicine. 8 (2020) 10 - p. , 2020
Link:
https://doi.org/10.1002/..
?
12
Identification of novel variants in Iranian consanguineous ..:
Bitarafan, Fatemeh
;
Seyedena, Seyed Yousef
;
Mahmoudi, Mahdi
.
Journal of Clinical Laboratory Analysis. 34 (2020) 12 - p. , 2020
Link:
https://doi.org/10.1002/..
?
13
A Genotype-First Approach for Clinical and Genetic Evaluati..:
Abbasi, Farzaneh
;
Habibi, Maryam
;
Enayati, Samaneh
...
Canadian Journal of Diabetes. 42 (2018) 3 - p. 272-275 , 2018
Link:
https://doi.org/10.1016/..
?
14
Isolated Congenital Anosmia and CNGA2 Mutation:
Sailani, M. Reza
;
Jingga, Inlora
;
MirMazlomi, Seyed Hashem
...
Scientific Reports. 7 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1038/..
?
15
Molecular investigation of WFS1 gene exon 8 in Iranian pati..:
Abbasi, Roshanak
;
Bitarafan, Fatemeh
;
Khodaeian, Mehrnoosh
...
International Journal of Diabetes in Developing Countries. 36 (2015) 1 - p. 75-80 , 2015
Link:
https://doi.org/10.1007/..
1-15