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Hemoglobin
international journal for hemoglobin research
Volume 24, 2000 - Issue 4
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Original Article

Homozygous HB Sallanches [α104(G11)CYS→TYR] in a Pakistani Child with HB H Disease

J. S. Waye Provincial Hemoglobinopathy DNA Diagnostic, Laboratory Hamillon Healih Sciences Coryoration, Hamilton, Ontario, Canada, L8N 325; Department of Pathology and Molecular, Medicine McMaster University, Hamilton, Ontario, Canada, L8N 325Correspondencewavei@,fhs.mcmaster.ca
,
L. Walker Provincial Hemoglobinopathy DNA Diagnostic, Laboratory Hamillon Healih Sciences Coryoration, Hamilton, Ontario, Canada, L8N 325
,
D. H. K. Chui Provincial Hemoglobinopathy DNA Diagnostic, Laboratory Hamillon Healih Sciences Coryoration, Hamilton, Ontario, Canada, L8N 325; Department of Pathology and Molecular, Medicine McMaster University, Hamilton, Ontario, Canada, L8N 325
,
J. Lafferty St. Joseph's Hospital, Hamilton, Ontario, Canada, L8N 4A6
&
M. Kirby The Hospital. for Sick Children, Toronto, Ontario, Canada, M5G 1-8
Pages 355-357 | Received 24 Apr 2000, Accepted 19 Jul 2000, Published online: 07 Jul 2009

Citations (12)

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Read on this site (6)

Prashant Warang, Sona Nair, Anita Nadkarni, Kanjaksha Ghosh & Roshan B. Colah. (2010) Hb H Disease Due to Homozygosity for a Rare α2-Globin Variant, Hb Sallanches. Hemoglobin 34:1, pages 45-48.
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Papai Roy, Gargi Bhattacharya, Debasish Banerjee, Sarmila Chandra, Malay Ghosh, Utpal Choudhuri, Manikanchan Das & Uma B. Dasgupta. (2009) Hb Sallanches [α104(G11)Cys→Tyr, TGC>TAC] Occurs Frequently on the Indian Subcontinent. Hemoglobin 33:6, pages 486-491.
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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.
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Sumitra Dash, Keiko Harano & Santosh Menon. (2006) Hb Sallanches [α104(G11)Cys→Tyr, TGC→TAC (α2)]: An Unstable Hemoglobin Variant Found in an Indian Child. Hemoglobin 30:3, pages 393-396.
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David H. K. Chui. (2005) Alpha-thalassaemia and population health in Southeast Asia. Annals of Human Biology 32:2, pages 123-130.
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Cornelis L. Harteveld, Lieke Rozendaal, Nico A. Blom, Shirley Lo-A-Njoe, Nicole Akkerman, Sandra Arkestijn, Peter Van Delft & Piero C. Giordano. (2005) Hb Oegstgeest [α104(G11)Cys → Ser (α1)]. A New Hemoglobin Variant Associated with a Mild α-Thalassemia Phenotype. Hemoglobin 29:3, pages 165-169.
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Articles from other publishers (6)

Samaneh Farashi & Hossein Najmabadi. (2015) Diagnostic pitfalls of less well recognized HbH disease. Blood Cells, Molecules, and Diseases 55:4, pages 387-395.
Crossref
Anita H. Nadkarni, Sona B. Nair, Khushnooma Y. Italia, Prashant Warang, Madhura Dalvi, Kanjaksha Ghosh & Roshan B. Colah. (2010) Molecular Diversity of Hemoglobin H Disease in India. American Journal of Clinical Pathology 133:3, pages 491-494.
Crossref
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallDouglas R. Higgs. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 266 295 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallDouglas R. Higgs. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 239 240 .
DAVID H.K. CHUI. (2009) α‐Thalassemia: Hb H Disease and Hb Barts Hydrops Fetalis. Annals of the New York Academy of Sciences 1054:1, pages 25-32.
Crossref
David H. K. ChuiSuthat FucharoenVivian Chan. (2003) Hemoglobin H disease: not necessarily a benign disorder. Blood 101:3, pages 791-800.
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