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Hemoglobin
international journal for hemoglobin research
Volume 22, 1998 - Issue 1
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Original Article

HB Tak Confirmed by DNA Analysis: Not Expressed as Thalassemia in a HB TAK/HB E Compound Heterozygote

J. D. Hoyer Department of Laboratory Medicine, Pathology Mayo Clinic, Rochester, MN, 55905, USA
,
M. J. Wick Department of Laboratory Medicine, Pathology Mayo Clinic, Rochester, MN, 55905, USA
,
S. N. Thibodeau Department of Laboratory Medicine, Pathology Mayo Clinic, Rochester, MN, 55905, USA
,
K. A. Viker Department of Laboratory Medicine, Pathology Mayo Clinic, Rochester, MN, 55905, USA
,
R. Conner Clinical Pathology Associates, Austin, TX, 78767, USA
&
V. F. Fairbanks Department of Laboratory Medicine, Pathology Mayo Clinic, Rochester, MN, 55905, USA
Pages 45-52 | Received 12 May 1997, Accepted 16 Oct 1997, Published online: 07 Jul 2009

Citations (14)

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Read on this site (4)

Fuanglada Tongprasert, Pimlak Charoenkwan, Kasemsri Srisupundit & Adisak Tantiworawit. (2017) Secondary erythrocytosis caused by hemoglobin Tak/β0-thalassaemia disease during pregnancy: A case report. Journal of Obstetrics and Gynaecology 37:2, pages 252-253.
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Nattiya Teawtrakul, Chittima Sirijirachai, Ganjana Chansung & Goonnapa Fucharoen. (2010) Compound Heterozygous Hb Tak/Hb E Causes Secondary Erythrocytosis in a Thai Family. Hemoglobin 34:2, pages 165-168.
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Mu-Chin Shih, Kang-His Wu, Su-Ching Liu & Jan-Gowth Chang. (2005) Hb Tak: A β Chain Elongation at the End of the β Chain, in a Taiwanese. Hemoglobin 29:1, pages 65-67.
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Giovanni Ivaldi, Onorata David, Maria Baffico, Daniela Leone, Maurizia Baldi, Maria Isola Parodi, Valeria Scimè‐Degani, Antonio Piga, Paola Scagni, Emma Rabino‐Massa & Giuseppe Ricco. (2003) Hb Trento: An Elongated C‐Terminal β Chain Due to a New Frameshift Mutation [β144 (−A)]. Hemoglobin 27:1, pages 15-25.
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Articles from other publishers (10)

Barbara J. Bain. 2020. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 261 324 .
John R. A. Shepherd, Paolo B. Dominelli, Tuhin K. Roy, Timothy W. Secomb, James D. Hoyer, Jennifer L. Oliveira & Michael J. Joyner. (2019) Modelling the relationships between haemoglobin oxygen affinity and the oxygen cascade in humans. The Journal of Physiology 597:16, pages 4193-4202.
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Jennifer L. Oliveira, Lea M. Coon, Lori A. Frederick, Molly Hein, Kenneth C. Swanson, Michelle E. Savedra, Tavanna R. Porter, Mrinal M. Patnaik, Ayalew Tefferi, Animesh Pardanani, Stefan K. Grebe, David S. Viswanatha & James D. Hoyer. (2018) Genotype-phenotype correlation of hereditary erythrocytosis mutations, a single center experience. American Journal of Hematology 93:8, pages 1029-1041.
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Jennifer L. Oliveira. (2018) Diagnostic Strategies in Hemoglobinopathy Testing, the Role of a Reference Laboratory in the USA. Thalassemia Reports 8:1, pages 7476.
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Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallSuthat Fucharoen & David J. Weatherall. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 417 434 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. Weatherall. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 321 322 .
Noppacharn Uaprasert, Ponlapat Rojnuckarin, Rung Settapiboon, Supaporn Amornsiriwat & Pranee Sutcharitchan. (2009) Clinical and hematological characteristics of uncommon beta-globin variants in Thailand. International Journal of Hematology 89:5, pages 568-571.
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Sonny O. Ang & Josef T. Prchal. 2007. Myeloproliferative Disorders. Myeloproliferative Disorders 297 319 .
. 2006. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 190 233 .
Voravarn S. Tanphaichitr, Vip Viprakasit, Gavivann Veerakul, Kleebsabai Sanpakit & Panutsaya Tientadakul. (2003) Homozygous Hemoglobin Tak Causes Symptomatic Secondary Polycythemia in a Thai Boy. Journal of Pediatric Hematology/Oncology 25:3, pages 261-265.
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