Advanced search
Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 21, 1997 - Issue 4
Submit an article Journal homepage
79
Views
18
CrossRef citations to date
0
Altmetric
Original Article

HB Seal Rock [(α2)142 Term→glu, Codon 142 TAA→GAA]: An Extended α Chain Variant Associated with Anemia, Microcytosis, and α-Thalassemia-2 (-3.7 KB)

D. Merritt Department of Obstetrics and Gynecology, Washington University School of Medicine, St Louis, MO, 63110, USA
,
R. T. Jones Department of Biochemistry, Oregon Health Sciences University, Portland, OR, 97201-3098, USA
,
C. Head Department of Biochemistry, Oregon Health Sciences University, Portland, OR, 97201-3098, USA
,
S. N. Thibodeau Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA
,
V. F. Fairbanks Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA
,
M. H. Steinberg Department of Medicine, Veterans Administration Medical Center, Jackson, MS, 39216, USA
,
M. B. Coleman Department of Medicine, Veterans Administration Medical Center, Jackson, MS, 39216, USA
&
G. P. Rodgers Molecular Hematology Unit, Laboratory of Chemical Biology National Institutes of Health, Bethesda, MD, 20892, USA
 show all
Pages 331-344 | Received 10 Feb 1997, Accepted 22 Apr 1997, Published online: 07 Jul 2009

Citations (18)

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

Subscribe to citation updates

Read on this site (5)

Hua Jiang, Lv-Yin Huang, Li Zhen, Fan Jiang & Dong-Zhi Li. (2017) Two α1-Globin Gene Point Mutations Causing Severe Hb H Disease. Hemoglobin 41:4-6, pages 293-296.
Read now
Henri Wajcman, Jan Traeger-Synodinos, Ioannis Papassotiriou, Piero C. Giordano, Cornelis L. Harteveld, Véronique Baudin-Creuza & John Old. (2008) Unstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia. Hemoglobin 32:4, pages 327-349.
Read now
T. H.J. Huisman & M. F.H. Carver. (1998) The Thalassemia Repository (Ninth Edition; Part II). Hemoglobin 22:3, pages 287-310.
Read now
J. Hitchen, A. McFarlane, J. Lafferty & M. A.M. Ali. (1998) Detection of α2- and α1- Globin Gene Variants by a Modified Cycle Sequencing Method. Hemoglobin 22:4, pages 373-376.
Read now
M. F. H. Carver & T. H. J. Huisman. (1997) International Hemoglobin Information Center Variant List. Hemoglobin 21:6, pages 505-506.
Read now

Articles from other publishers (13)

Pallavi Thaker, Namrata Mahajan, Malay B. Mukherjee & Roshan B. Colah. (2022) Molecular Heterogeneity of Hb H Disease in India. Thalassemia Reports 12:3, pages 73-84.
Crossref
Matthieu Deltombe, Meryem Benamour, Isabelle Derclaye & Diane Maisin. (2022) Detection of hemoglobin Kinshasa by a capillary electrophoresis method. Clinica Chimica Acta 531, pages 81-83.
Crossref
Roshan B. Colah, Anita Nadkarni, Ajit Gorakshakar, Pratibha Sawant, Manju Gorivale, Pallavi Mehta, Madhavi Sawant & Kanjaksha Ghosh. (2016) Five Rare β Globin Chain Hemoglobin Variants in India. Indian Journal of Hematology and Blood Transfusion 32:S1, pages 282-286.
Crossref
Samaneh Farashi & Hossein Najmabadi. (2015) Diagnostic pitfalls of less well recognized HbH disease. Blood Cells, Molecules, and Diseases 55:4, pages 387-395.
Crossref
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. Weatherall. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 241 265 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallDouglas R. Higgs. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 239 240 .
Andreas E. Kulozik. 2006. Pediatric Hematology. Pediatric Hematology 231 254 .
Easaw Thomas, George S.H. Yeo & Tony Y.T. Tan. 2004. Anesthetic and Obstetric Management of High-Risk Pregnancy. Anesthetic and Obstetric Management of High-Risk Pregnancy 253 264 .
D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Andreas E. Kulozik. 2000. Monogen bedingte Erbkrankheiten 1. Monogen bedingte Erbkrankheiten 1 369 392 .
A. AmeriV.F. FairbanksG.A. YanikF. MahdiS.N. ThibodeauD.J. McCormickL.A. BoxerK.T. McDonagh. (1999) Identification of the Molecular Genetic Defect of Patients With Methemoglobin M Kankakee (M-Iwate), 87 (F8) His → Tyr: Evidence for an Electrostatic Model of M Hemoglobin Assembly. Blood 94:5, pages 1825-1826.
Crossref
A. AmeriV.F. FairbanksG.A. YanikF. MahdiS.N. ThibodeauD.J. McCormickL.A. BoxerK.T. McDonagh. (1999) Identification of the Molecular Genetic Defect of Patients With Methemoglobin M Kankakee (M-Iwate), 87 (F8) His → Tyr: Evidence for an Electrostatic Model of M Hemoglobin Assembly. Blood 94:5, pages 1825-1826.
Crossref
Luigi F. Bernini & Cornelis L. Harteveld. (1998) 2 α-Thalassaemia. Baillière's Clinical Haematology 11:1, pages 53-90.
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:

Order Reprints Request Corporate Permissions

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:

Request Academic Permissions

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.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.