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Items: 10

1.

Characterization and haplotype study of 6 novel STR markers related to the KCNQ1 gene in heterogeneous cardiovascular disorders in the Iranian population

Amirian A, Zafari Z, Sharifi Z, Kordafshari A, Karimipoor M, Zeinali S.

Turk J Med Sci. 2019 Apr 18;49(2):453-457. doi: 10.3906/sag-1805-43.

PMID:
30866607
2.

Identification of a Novel KCNQ1 Frameshift Mutation and Review of the Literature among Iranian Long QT Families

Amirian A, Zafari Z, Karimipoor M, Kordafshari A, Dalili M, Saber S, Farjam Fazelifar A, Zeinali S.

Iran Biomed J. 2019 May;23(3):228-34. Epub 2019 Feb 24. Review.

3.

Detection of a new KCNQ1 frameshift mutation associated with Jervell and Lange-Nielsen syndrome in 2 Iranian families.

Amirian A, Zafari Z, Dalili M, Saber S, Karimipoor M, Dabbagh Bagheri S, Fazelifar AF, Zeinali S.

J Arrhythm. 2018 Apr 16;34(3):286-290. doi: 10.1002/joa3.12042. eCollection 2018 Jun.

4.

Development and diversity of a novel panel of short tandem repeat markers encompassing the SCN5Agene in Iranian population.

Zafari Z, Amirian A, Nejad FR, Akbari V, Akbari MT, Zeinali S.

J Genet. 2018 Apr 11;97(1):e49-e52. No abstract available.

5.

Novel frameshift mutation in the KCNQ1 gene responsible for Jervell and Lange-Nielsen syndrome.

Amirian A, Dalili SM, Zafari Z, Saber S, Karimipoor M, Akbari V, Fazelifar AF, Zeinali S.

Iran J Basic Med Sci. 2018 Jan;21(1):108-111. doi: 10.22038/IJBMS.2017.23207.5908.

6.

Molecular Characterization of δ-Thalassemia in Iran.

Kordafshari A, Amirian A, Zeinali S, Valaei A, Maryami F, Karimipoor M.

Hemoglobin. 2016;40(1):44-7. doi: 10.3109/03630269.2015.1092982.

PMID:
26754299
7.

The carrier frequency of α-globin gene triplication in an Iranian population with normal or borderline hematological parameters.

Moosavi SF, Amirian A, Zarbakhsh B, Kordafshari A, Mirzahoseini H, Zeinali S, Karimipoor M.

Hemoglobin. 2011;35(4):323-30. doi: 10.3109/03630269.2011.571527.

PMID:
21797699
8.

Co-inheritance of hemoglobin D and β-thalassemia traits in three Iranian families: clinical relevance.

Taghavi Basmanj M, Karimipoor M, Amirian A, Jafarinejad M, Katouzian L, Valaei A, Bayat F, Kordafshari A, Zeinali S.

Arch Iran Med. 2011 Jan;14(1):61-3. doi: 011141/AIM.0014.

9.

First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia with delta globin CD12 {Asn-->Lys (AAT-->AAA)}HbA₂-NYU in Iran.

Amirian A, Karimipoor M, Jafarinejad M, Taghavi M, Kordafshari A, Fathi Azar S, Mohammadi MS, Zeinali S.

Arch Iran Med. 2011 Jan;14(1):8-11. doi: 011141/AIM.003.

10.

Identification of a novel δ-globin gene mutation in an Iranian family.

Amirian A, Jafarinejad M, Kordafshari AR, Mosayyebzadeh M, Karimipoor M, Zeinali S.

Hemoglobin. 2010;34(6):594-8. doi: 10.3109/03630269.2010.528323.

PMID:
21077769

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