E-LIB Suche - Ergebnisse für: Masomeh Askari

1

A novel missense variant in CDK5RAP2 associated with non-ob..:

Rahimian, Mouness ; Askari, Masomeh ; Salehi, Najmeh...
Taiwanese Journal of Obstetrics and Gynecology. 62 (2023) 6 - p. 830-837 , 2023

Link: https://doi.org/10.1016/..

2

A systematic review and meta-analysis for the association o..:

Cheraghpour, Makan ; Askari, Masomeh ; Tierling, Sascha...
Frontiers in Oncology. 13 (2023) - p. , 2023

Link: https://doi.org/10.3389/..

3

A rare frameshift mutation inSYCP1is associated with human ..:

Nabi, Soheila ; Askari, Masomeh ; Rezaei-Gazik, Maryam...
Molecular Human Reproduction. 28 (2022) 4 - p. , 2022

Link: https://doi.org/10.1093/..

4

Prediction and interpretation of rare missense variant in O..:

Askari, Masomeh ; Moradi, Zahra ; Mohammadi, Mahsa..
Genomics. 113 (2021) 4 - p. 2793-2799 , 2021

Link: https://doi.org/10.1016/..

5

Targeted sequencing of CDH23 and GJB2 genes in an Iranian p..:

Torkamandi, Shahram ; Bayat, Sahar ; Mirfakhraie, Reza...
Gene Reports. 23 (2021) - p. 101149 , 2021

Link: https://doi.org/10.1016/..

6

Whole exome sequencing identified two homozygous ALMS1 muta..:

Torkamandi, Shahram ; Rezaei, Somaye ; Mirfakhraei, Reza...
Gene. 727 (2020) - p. 144228 , 2020

Link: https://doi.org/10.1016/..

7

Testis formation in XX individuals resulting from novel pat..:

Eozenou, Caroline ; Gonen, Nitzan ; Touzon, Maria Sol...
Proceedings of the National Academy of Sciences. 117 (2020) 24 - p. 13680-13688 , 2020

Link: https://doi.org/10.1073/..

8

Testis formation in XX individuals resulting from novel pat..:

Eozenou, Caroline ; Gonen, Nitzan ; Touzon, Maria Sol...
Proceedings of the National Academy of Sciences of the United States of America. 117 (2020) 24 - p. 13680-13688 , 2020

Link: https://www.jstor.org/st..

9

A missense mutation inNR5A1causing female to male sex rever..:

Askari, Masomeh ; Rastari, Mandana ; Seresht‐Ahmadi, Mehrshad...
Andrologia. 52 (2020) 6 - p. , 2020

Link: https://doi.org/10.1111/..

10

Novel MYO15A variants are associated with hearing loss in t..:

Khatami, Somayeh ; Askari, Masomeh ; Bahreini, Fatemeh...
BMC Medical Genetics. 21 (2020) 1 - p. , 2020

Link: https://doi.org/10.1186/..

11

Rare case of an oligospermic male with 46,XX/46,XY tetragam..:

Magharehabed, Mahshad ; Almadani, Navid ; Askari, Masomeh...
Andrologia. 51 (2019) 7 - p. , 2019

Link: https://doi.org/10.1111/..

12

Identification of a homozygous GFPT2 variant in a family wi..:

Askari, Masomeh ; Kordi-Tamandani, Dor Mohammad ; Almadani, Navid..
Gene. 699 (2019) - p. 16-23 , 2019

Link: https://doi.org/10.1016/..

13

Identification of a missense variant in CLDN2 in obstructiv..:

Askari, Masomeh ; Karamzadeh, Razieh ; Ansari-Pour, Naser...
Journal of Human Genetics. 64 (2019) 10 - p. 1023-1032 , 2019

Link: https://doi.org/10.1038/..

14

Table_1_A systematic review and meta-analysis for the assoc..:

Makan Cheraghpour ; Masomeh Askari ; Sascha Tierling...
doi:10.3389/fonc.2023.1168942.s001. , 2023

Link: https://doi.org/10.3389/..

15

A systematic review and meta-analysis for the association o..:

Makan Cheraghpour ; Masomeh Askari ; Sascha Tierling...
https://www.frontiersin.org/articles/10.3389/fonc.2023.1168942/full. , 2023

Link: https://doi.org/10.3389/..