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Hemoglobin
international journal for hemoglobin research
Volume 30, 2006 - Issue 3
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SHORT COMMUNICATION

Hb Sallanches [α104(G11)Cys→Tyr, TGC→TAC (α2)]: An Unstable Hemoglobin Variant Found in an Indian Child

Sumitra Dash Department of Haematology, Post Graduate Institute of Medical Education and Research, Chandigarh, IndiaCorrespondence[email protected]
,
Keiko Harano Department of Clinical Nutrition, Kawasaki University of Medical Welfare, Kurashiki, Japan
&
Santosh Menon Department of Haematology, Post Graduate Institute of Medical Education and Research, Chandigarh, India
Pages 393-396 | Received 09 Dec 2005, Accepted 27 Jan 2006, Published online: 07 Jul 2009

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Loïc Garçon, Achille Iolascon, Serge Pissard, Maria R. Esposito, Roberta Russo, Odile Fenneteau, Madeleine Fénéant-Thibault, Hermann Heimpel & Jean Delaunay. (2010) A Dyserythropoietic Anemia Associated with Homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), A Variant with an Unstable α Chain. Hemoglobin 34:6, pages 576-581.
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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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Varvara Douna, Ioannis Papassotiriou, Anastasia Garoufi, Eleni Georgouli, Vassilis Ladis, Alexandra Stamoulakatou, Anna Metaxotou-Mavrommati, Emmanuel Kanavakis & Joanne Traeger-Synodinos. (2008) A Rare Thalassemic Syndrome Caused by Interaction of Hb Adana [α59(E8)Gly→Asp] with an α+-Thalassemia Deletion: Clinical Aspects in Two Cases. Hemoglobin 32:4, pages 361-369.
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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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Articles from other publishers (3)

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.
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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.
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Thanyachai Sura, Objoon Trachoo, Vip Viprakasit, Prin Vathesatogkit, Atchara Tunteeratum, Manisa Busabaratana, Raewadee Wisedpanichkij & Parttraporn Isarangkura. (2007) Hemoglobin H disease induced by the common SEA deletion and the rare hemoglobin Quong Sze in a Thai female: longitudinal clinical course, molecular characterization, and development of a PCR/RFLP-based detection method. Annals of Hematology 86:9, pages 659-663.
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