E-LIB Suche - Ergebnisse für: Bagherian, Hamideh

1

Identification and in silico structural analysis for the fi..:

Hosseini Nami, Amin ; Kabiri, Mahboubeh ; Zafarghandi Motlagh, Fatemeh...
Therapeutic Advances in Respiratory Disease. 18 (2024) - p. , 2024

Link: https://doi.org/10.1177/..

2

First report of a patient with homozygous hemoglobin Ernz: ..:

Shojaei, Zohreh ; Abiri, Maryam ; Zafarghandi Motlagh, Fatemeh...
Blood Cells, Molecules, and Diseases. 104 (2024) - p. 102797 , 2024

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

3

Genetic attributes of Iranian cystic fibrosis patients: the..:

Hosseini Nami, Amin ; Kabiri, Mahboubeh ; Zafarghandi Motlagh, Fatemeh...
Frontiers in Genetics. 14 (2023) - p. , 2023

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

4

A decade of molecular preimplantation genetic diagnosis of ..:

Keshvar, Yeganeh ; Sabeghi, Solmaz ; Sharifi, Zohreh...
BMC Pregnancy and Childbirth. 22 (2022) 1 - p. , 2022

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

5

Mutational screening through comprehensive bioinformatics a..:

Ghadamyari, Faranak ; Heidari, Mohammad Mehdi ; Zeinali, Sirous...
Journal of Clinical Laboratory Analysis. 35 (2021) 5 - p. , 2021

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

6

Autozygosity Mapping by Genome-wide Single Nucleotide Polym..:

Zeinali, Sirous ; Youssefian, Leila ; Vahidnezhad, Hassan...
International Journal of Dermatology and Venereology. 4 (2021) 2 - p. 82-85 , 2021

Link: https://doi.org/10.1097/..

7

Biallelic variants in MESD, which encodes a WNT-signaling-r..:

Tran, Thao T. ; Keller, Rachel B. ; Guillemyn, Brecht...
Human Genetics and Genomics Advances. 2 (2021) 4 - p. 100051 , 2021

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

8

Comprehensive Mutation Analysis and Report of 12 Novel Muta..:

Sharifi, Zohreh ; Taheri, Mohammad ; Fallah, Mohammad-Sadegh...
Journal of Molecular Neuroscience. 71 (2021) 11 - p. 2281-2298 , 2021

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

9

Molecular genetic study of Calpainopathy in Iran:

Mojbafan, Marzieh ; Khajeh, Ali ; Habibi, Haleh..
Gene. 677 (2018) - p. 259-265 , 2018

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

10

Molecular genetics of a cohort of 635 cases of phenylketonu..:

Shirzadeh, Tina ; Saeidian, Amir Hossein ; Bagherian, Hamideh...
Journal of Inherited Metabolic Disease. 41 (2018) 6 - p. 1159-1167 , 2018

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

11

Autozygosity mapping of methylmalonic acidemia associated g..:

Shafaat, Mehdi ; Alaee, Mohammad Reza ; Rahmanifar, Ali...
Metabolic Brain Disease. 33 (2018) 5 - p. 1689-1697 , 2018

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

12

Cryptic de novo deletion at 2q23.3-q24.1 in a patient with ..:

MALBIN, JAMILEH ; FALLAH, MOHAMMAD-SADEGH ; SHARIFI, ZOHREH...
Journal of Genetics. 95 (2016) 2 - p. 441-445 , 2016

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

13

Identification of six novel mutations in Iranian patients w..:

Abiri, Maryam ; Karamzadeh, Razieh ; Karimipoor, Morteza...
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 786 (2016) - p. 34-40 , 2016

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

14

GJB2 c.−23+1G>A mutation is second most common mutation amo..:

Zeinali, Sirous ; Davoudi-Dehaghani, Elham ; Azadmehr, Sarah...
European Archives of Oto-Rhino-Laryngology. 272 (2014) 9 - p. 2255-2259 , 2014

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

15

A transversion mutation in non-coding exon 3 of the TMC1 ge..:

Davoudi-Dehaghani, Elham ; Zeinali, Sirous ; Mahdieh, Nejat...
International Journal of Pediatric Otorhinolaryngology. 77 (2013) 5 - p. 821-826 , 2013

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