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Hemoglobin
international journal for hemoglobin research
Volume 29, 2005 - Issue 4
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Short Communication

High Incidence of Hb D-Los Angeles [β121(GH4)Glu→Gln] in Denizli Province, Aegean Region of Turkey

Erol Ö. Atalay Department of Biophysics, Medical Faculty, Pamukkale University, Denizli, Turkey; Pamukkale University Research Center for Genetic Engineering and Biotechnology, Denizli, TurkeyCorrespondence[email protected]
, Ph.D.,
Hasan Koyuncu Turkish Ministry of Health, Denizli Hemoglobinopathy Center, Denizli, Turkey
,
Berna Turgut Turkish Ministry of Health, Denizli Hemoglobinopathy Center, Denizli, Turkey
,
Ayfer Atalay Department of Biophysics, Medical Faculty, Pamukkale University, Denizli, Turkey; Pamukkale University Research Center for Genetic Engineering and Biotechnology, Denizli, Turkey
,
Sanem Yildiz Department of Biophysics, Medical Faculty, Pamukkale University, Denizli, Turkey; Pamukkale University Research Center for Genetic Engineering and Biotechnology, Denizli, Turkey
,
Anzel Bahadir Department of Biophysics, Medical Faculty, Pamukkale University, Denizli, Turkey; Pamukkale University Research Center for Genetic Engineering and Biotechnology, Denizli, Turkey
&
Aylin Köseler Department of Biophysics, Medical Faculty, Pamukkale University, Denizli, Turkey; Pamukkale University Research Center for Genetic Engineering and Biotechnology, Denizli, Turkey
 show all
Pages 307-310 | Received 02 Jun 2005, Accepted 01 Jul 2005, Published online: 07 Jul 2009

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Ahmet Genc, Deniz Tastemir Korkmaz, Mehmet Buyukleyla & Murat Celiker. (2012) Prevalence and Molecular Analysis of β-Thalassemia in Adiyaman, Turkey. Hemoglobin 36:2, pages 131-138.
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Ayfer Atalay, Hasan Koyuncu, Aylin Köseler, Anzel Ozkan & Erol Ö. Atalay. (2007) Hb Beograd [β121(GH4)Glu→Val, GAA→GTA] in the Turkish Population. Hemoglobin 31:4, pages 491-493.
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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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Erol Ö. Atalay, Emre Üstel, Sanem Yildiz & Ayfer Atalay. (2006) Surface Plasmon Resonance-Based Molecular Detection of Hb S [β6(A3)Glu→Val, GAG→GTG] at the Gene Level. Hemoglobin 30:3, pages 385-391.
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Articles from other publishers (14)

Cameron Heaton, Matthias Witt, Laura Cole, Jason Eyre, Simon Tazzyman, Richard McColm & Simona Francese. (2021) Detection and mapping of haemoglobin variants in blood fingermarks by MALDI MS for suspect “profiling”. The Analyst 146:13, pages 4290-4302.
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Deniz Aslan. (2020) Is Hemoglobin D Trait Hematologically Silent: Comparison With Healthy Controls and β-thalassemia Carriers. Journal of Pediatric Hematology/Oncology 42:7, pages e698-e701.
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ZuhairAbd Ali Al-Barazanchi, SubehSalim Abdulateef, MeaadKadhum Hassan & RawshanZuhair Jaber. (2019) Double heterozygosity for hemoglobin S and D Punjab in Basra, Iraq: A Clinical and hematological study of 42 patients. Journal of Applied Hematology 10:4, pages 134.
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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. (2018) Estimating the age of Hb G-Coushatta [β22(B4)Glu→Ala] mutation by haplotypes of β-globin gene cluster in Denizli, Turkey. Molecular Genetics & Genomic Medicine 6:4, pages 547-554.
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Waqar A. Khan, Bilquis Banu, Salma Sadiya & Golam Sarwardi. (2017) Spectrum of Types of Thalassemias and Hemoglobinopathies: Study in a Tertiary Level Children Hospital in Bangladesh. Thalassemia Reports 7:1, pages 6354.
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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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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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Aylin Köseler, Onur Öztürk, Ayfer Atalay & Erol Ö. Atalay. (2012) Molecular Studies on the Origin of the Hb G-Coushatta Mutation in Denizli Province of Turkey. Biochemical Genetics 51:1-2, pages 71-75.
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Aylin Köseler, Onur Öztürk, Ayfer Atalay & Erol Ö. Atalay. (2012) Allele frequency of VNTR locus D1S80 observed in Hb D-Los Angeles carrires. Molecular Biology Reports 39:12, pages 10747-10750.
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Sanjay Pandey, Rahasya Mani Mishra, Sweta Pandey, Vineet Shah & Renu Saxena. (2012) Molecular characterization of hemoglobin D Punjab traits and clinical-hematological profile of the patients. Sao Paulo Medical Journal 130:4, pages 248-251.
Crossref
Ahmad A. Mallouh. 2012. Textbook of Clinical Pediatrics. Textbook of Clinical Pediatrics 3023 3027 .
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.
Crossref
Aylin Köseler, Ayfer Atalay & Erol Ömer Atalay. (2009) Allele Frequency of VNTR Locus D1S80 Observed in Denizli Province of Turkey. Biochemical Genetics 47:7-8, pages 540-546.
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