Citations (18)
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Sheila Das & Ranjeet S. Mashon. (2015) Coinheritance of Hb D-Punjab and β-Thalassemia: Diagnosis and Implications in Prenatal Diagnosis. Hemoglobin 39:2, pages 138-140.
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Dilip K. Patel, Ranjeet S. Mashon, Siris Patel, Preetinanda M. Dash & Bhabani S. Das. (2010) β-Globin Gene Haplotypes Linked with the Hb D-Punjab [β121(GH4)Glu→Gln, GAA>CAA] Mutation in Eastern India. Hemoglobin 34:6, pages 530-537.
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Erol Ö. Atalay, Ayfer Atalay, Emre Üstel, Sanem Yildiz, Onur Öztürk, Aylin Köseler & Anzel Bahadir. (2007) Genetic Origin of Hb D-Los Angeles [β121(GH4)Glu→Gln, GAA→CAA] According to the β-Globin Gene Cluster Haplotypes. Hemoglobin 31:3, pages 387-391.
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Articles from other publishers (15)
Negin Rezavand, Saba Tabarok, Ziba Rahimi, Asad Vaisi‐Raygani, Ehsan Mohammadi & Zohreh Rahimi. (2018) The effect of VDR gene polymorphisms and vitamin D level on blood pressure, risk of preeclampsia, gestational age, and body mass index. Journal of Cellular Biochemistry 120:4, pages 6441-6448.
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Kheirollah Yari & Zohreh Rahimi. (2019) Promoter Methylation Status of the Retinoic Acid Receptor-Beta 2 Gene in Breast Cancer Patients: A Case Control Study and Systematic Review. Breast Care 14:2, pages 117-123.
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Onur Ozturk, Sanem Arikan, Ayfer Atalay & Erol O. Atalay. (2018) Time estimations by network of beta globin gene cluster haplotypes linked with Hb D-Los Angeles [β121 (GH4) Glu → Gln GAA → CAA] mutation in the world populations. Molecular Genetics & Genomic Medicine 6:6, pages 1181-1187.
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Onur Ozturk, Sanem Arikan, Ayfer Atalay & Erol O. Atalay. (2016)
Analysis of the population genetic structure of Hb D-Los Angeles [β121 (GH4) Glu→Gln
G
AA→
C
AA] in Denizli, Turkey; genetic diversity, historical demography and estimation of the mutation rates based on haplotype variation
. American Journal of Human Biology 28:4, pages 476-483.
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Sahar Mohammadi, Habibolah Khazaie, Ziba Rahimi, Asad Vaisi-Raygani, Newsha Zargooshi & Zohreh Rahimi. (2015) The serotonin transporter (5-HTTLPR) but not serotonin receptor (5-HT2C Cys23Ser) variant is associated with bipolar I disorder in Kurdish population from Western Iran. Neuroscience Letters 590, pages 91-95.
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Lidiane de Souza Torres, Jéssika Viviani Okumura, Danilo Grünig Humberto da Silva & Claudia Regina Bonini-Domingos. (2015) Hemoglobin D-Punjab: origin, distribution and laboratory diagnosis. Revista Brasileira de Hematologia e Hemoterapia 37:2, pages 120-126.
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Mohammad Reza Mahdavi, Hossein Jalali, Mehrnoush Kosaryan, Payam Roshan & Mehrad Mahdavi. (2015) β-Globin gene cluster haplotypes of Hb D-Los Angeles in Mazandaran Province, Iran. Genes & Genetic Systems 90:1, pages 55-57.
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Ziba Rahimi, Leila Kazemian, Shohreh Malek-Khosravi, Farid Najafi & Zohreh Rahimi. (2014) Matrix metalloproteinase-7 A-181G and its interaction with matrix metalloproteinase-9 C-1562T polymorphism in preeclamptic patients: association with malondialdehyde level and severe preeclampsia. Archives of Gynecology and Obstetrics 291:1, pages 45-51.
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Ziba Rahimi, Zohreh Rahimi, Fatemeh Mohammadi, Nazanin Razazian & Farid Najafi. (2014) Association of matrix metalloproteinase-7A-181G variants with the risk of multiple sclerosis. Personalized Medicine 11:8, pages 727-733.
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Zohreh Rahimi. (2013) Genetic Epidemiology, Hematological and Clinical Features of Hemoglobinopathies in Iran. BioMed Research International 2013, pages 1-10.
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Zohreh Rahimi, Zainab Ahmadian, Reza Akramipour, Asad Vaisi-Raygani, Ziba Rahimi & Abbas Parsian. (2011) Thymidylate synthase and methionine synthase polymorphisms are not associated with susceptibility to childhood acute lymphoblastic leukemia in Kurdish population from Western Iran. Molecular Biology Reports 39:3, pages 2195-2200.
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Ali Reza Rezaee, Mohammad Mehdi Banoei, Elham Khalili & Massoud Houshmand. (2012) Beta-Thalassemia in Iran: New Insight into the Role of Genetic Admixture and Migration. The Scientific World Journal 2012, pages 1-7.
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Zohreh RahimiReza Nourozi-RadAsad Vaisi-RayganiMohammad-Reza SaidiZiba RahimiReza AhmadiReza YaraniKoorosh HamzeheeAbbas Parsian. (2011) Association Between Cholesteryl Ester Transfer Protein TaqIB Variants and Risk of Coronary Artery Disease and Diabetes Mellitus in the Population of Western Iran. Genetic Testing and Molecular Biomarkers 15:11, pages 813-819.
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Zohreh Rahimi, Vahid Felehgari, Mehrali Rahimi, Hadi Mozafari, Kheirollah Yari, Asad Vaisi-Raygani, Mansour Rezaei, Shohreh Malek-Khosravi & Habibolah Khazaie. (2010) The frequency of factor V Leiden mutation, ACE gene polymorphism, serum ACE activity and response to ACE inhibitor and angiotensin II receptor antagonist drugs in Iranians type II diabetic patients with microalbuminuria. Molecular Biology Reports 38:3, pages 2117-2123.
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Zohreh Rahimi, Adriana Muniz & Hadi Mozafari. (2009) Abnormal hemoglobins among Kurdish population of Western Iran: hematological and molecular features. Molecular Biology Reports 37:1, pages 51-57.
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