E-LIB Suche - Ergebnisse für: Mohammad Yahya Vahidi Mehrjardi

1

Characterizing Homozygous Variants in Bardet-Biedl Syndrome..:

Feizabadi, Masoumeh Heidari ; Alerasool, Masoome ; Eslahi, Atieh...
Biochemical Genetics. , 2024

Link: https://doi.org/10.1007/..

2

The association of RBX1 and BAMBI gene expression with oocy..:

Monshizadeh, Kimia ; Tajamolian, Masoud ; Anbari, Fatemeh...
BMC Medical Genomics. 17 (2024) 1 - p. , 2024

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

3

Corrigendum to "Evaluation of NF1 and RASA1 gene expression..:

Yarahmadi, Ghafour ; Dehghanian, Mehran ; Sandoghsaz, Reyhaneh Sadat...
European Journal of Obstetrics & Gynecology and Reproductive Biology: X. 17 (2023) - p. 100173 , 2023

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

4

GGPS1‐associated muscular dystrophy with and without hearin..:

Kaiyrzhanov, Rauan ; Perry, Luke ; Rocca, Clarissa...
Annals of Clinical and Translational Neurology. 9 (2022) 9 - p. 1465-1474 , 2022

Link: https://doi.org/10.1002/..

5

Evaluation of the relationship between miR-1271 and GRB2 ge..:

Yarahmadi, Ghafour ; Fazeli, Javad ; Dehghanian, Mehran...
European Journal of Obstetrics & Gynecology and Reproductive Biology. 277 (2022) - p. 12-15 , 2022

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

6

Testicular expression of TDRD1, TDRD5, TDRD9 and TDRD12 in ..:

Babakhanzadeh, Emad ; Khodadadian, Ali ; Rostami, Saadi...
BMC Medical Genetics. 21 (2020) 1 - p. , 2020

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

7

Pontocerebellar hypoplasia due to bi-allelic variants in MI..:

Appelhof, Bart ; Wagner, Matias ; Hoefele, Julia...
European Journal of Human Genetics. 29 (2020) 3 - p. 411-421 , 2020

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

8

The clinical spectrum of the congenital myasthenic syndrome..:

Rodríguez Cruz, Pedro M. ; Cossins, Judith ; de Paula Estephan, Eduardo...
Brain. 142 (2019) 6 - p. 1547-1560 , 2019

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

9

Clinical presentation and natural history of infantile-onse..:

Helal, Mayada ; Mazaheri, Neda ; Shalbafan, Bita...
Neurological Sciences. 39 (2018) 11 - p. 1917-1925 , 2018

Link: https://doi.org/10.1007/..

10

Potential role of gender specific effect of leptin receptor..:

Dehghani, Mohammad Reza ; Mehrjardi, Mohammad Yahya Vahidi ; Dilaver, Nafi...
European Journal of Medical Genetics. 61 (2018) 8 - p. 465-467 , 2018

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

11

B3GALNT2 mutations associated with non-syndromic autosomal ..:

Maroofian, Reza ; Riemersma, Moniek ; Jae, Lucas T....
Genome Medicine. 9 (2017) 1 - p. , 2017

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

12

A Common Ancestral Asn242Ser Mutation in TMEM67 Identified ..:

Dehghani, MohammadReza ; Mojarad, Majid ; Karimiani, Ehsan Ghayoor...
Public Health Genomics. 20 (2017) 3 - p. 188-193 , 2017

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

13

The association of RBX1 and BAMBI gene expression with oocy..:

Kimia Monshizadeh ; Masoud Tajamolian ; Fatemeh Anbari...
https://doi.org/10.1186/s12920-024-01800-2. , 2024

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

14

Presentation_1_Joint effects of paraoxonase 1 rs662 polymor..:

Mina Darand ; Amin Salehi-Abargouei ; Mohammad Yahya Vahidi Mehrjardi...
doi:10.3389/fnut.2022.1097411.s001. , 2023

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

15

Interaction of dietary patterns with rs28362491 on severity..:

Zahra Darabi ; Seyed Mostafa Seyed Hosseini ; Mohammadtaghi Sarebanhassanabadi...
https://doi.org/10.1038/s41598-023-41438-1. , 2023

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