616
Views
10
CrossRef citations to date
0
Altmetric
HEMOGLOBINOPATHY

Alpha thalassemia gene mutations in neonates from Mazandaran, Iran, 2012

, , , , &

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (1)

Hajar Eftekhari, Ahmad Tamaddoni, Hassan Mahmoudi Nesheli, Mohsen Vakili, Sadegh Sedaghat, Ali Banihashemi, Mandana Azizi, Reza Youssefi Kamangar & Haleh Akhavan-Niaki. (2017) A Comprehensive Molecular Investigation of α-Thalassemia in an Iranian Cohort from Different Provinces of North Iran. Hemoglobin 41:1, pages 32-37.
Read now

Articles from other publishers (9)

Hossein Jalali, Hossein Karami, Mahan Mahdavi & Mohammad Reza Mahdavi. (2023) HbAdrian (α1:c.251del, p.Leu84Argfs*19)—A Novel Pathogenic Variant in the α1-Globin Gene Associated with Microcytosis from the North of Iran. Thalassemia Reports 13:2, pages 152-156.
Crossref
Hossein Jalali, Hossein Karami, Mohammad Reza Mahdavi & Mehrad Mahdavi. (2022) Co-Inheritance of Heterozygous β0-Thalassemia with Single Functional α-Globin Gene: Challenges of Carrier Detection in Pre-Marital Screening Program for Thalassemia. Thalassemia Reports 12:3, pages 101-104.
Crossref
Hossein Jalali, Mohammad Reza Mahdavi, Mahan Mahdavi & Adeleh Abbasi. (2022) Hb Mazandaran (α1) α51 Gly > Cys(CE9), c.154 GGC > TGC: A Novel Haemoglobin Variant of α1-Globin Gene. Thalassemia Reports 12:3, pages 51-54.
Crossref
H. Jalali, S.T. Rasouli, M. Najafi, H. Karami, M.R. Mahdavi & M. Mahdavi. (2020) A report of Hb Fontainebleau [α21 (B2) Ala > Pro] as a result of founder effect phenomenon. Gene Reports 19, pages 100587.
Crossref
Bijan Keikhaei, Pejman Slehi-fard, Gholamreza Shariati & Abbas Khosravi. (2018) Genetics of Iranian Alpha-Thalassemia Patients: A Comprehensive Original Study. Biochemical Genetics 56:5, pages 506-521.
Crossref
Hadi Darvishi-Khezri, Ebrahim Salehifar, Mehrnoush Kosaryan, Hossein Karami, Abbas Alipour, Fatemeh Shaki & Aily Aliasgharian. (2017) The impact of silymarin on antioxidant and oxidative status in patients with β-thalassemia major: A crossover, randomized controlled trial. Complementary Therapies in Medicine 35, pages 25-32.
Crossref
Hossein Karami, Hossein Jalali, Mehrad Mahdavi & Mohammad Reza Mahdavi. (2017) Identification of a Neonate with Thalassemia Intermedia Despite Premarital Screening Program in Mazandaran Province (Co-inheritance of Hb Knossos and IVS II-1 G> A Mutations). Research in Molecular Medicine 5:2, pages 34-36.
Crossref
Hossein Jalali, Mehrnoush Kosaryan, Mohammad Reza Mahdavi & Mehrad Mahdavi. (2017) Co-inheritance of --MED double gene deletion and αααAnti3.7 triplication on α-globin gene in Mazandaran at 2016. Research in Molecular Medicine 5:1, pages 44-47.
Crossref
Faeghe Aghajani, Mohammad Reza Mahdavi, Mehrnoush Kosaryan, Mehrad Mahdavi, Mohaddase Hamidi & Hossein Jalali. (2016) Identification of β-globin haplotypes linked to sickle hemoglobin (Hb S) alleles in Mazandaran province, Iran. Genes & Genetic Systems 91:6, pages 311-313.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.