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Hemoglobin
international journal for hemoglobin research
Volume 29, 2005 - Issue 2
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Original Article

Hb Geldrop St. Anna [β94(FG1)Asp→Tyr]: a New Hemoglobin Variant Observed in a Diabetic Patient

Cornelis L. Harteveld The Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands
,
Marc H. M. Thelen Department of Clinical Chemistry, St. Anna Hospital, Geldrop, The Netherlands
,
Johannes J. A. Rutten Huisartspraktijk Rutten JJA, Nuenen, The Netherlands
,
Jolanda Leuverman Department of Clinical Chemistry, St. Anna Hospital, Geldrop, The Netherlands
,
Nicole Akkermans The Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands
,
Peter van Delft The Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands
,
Sandra Arkesteijn The Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands
&
Piero C. Giordano The Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Leiden, The NetherlandsCorrespondence[email protected]
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Pages 107-112 | Received 03 Dec 2004, Accepted 06 Jan 2005, Published online: 09 Nov 2010

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Judith O. Kaufmann, Marion Phylipsen, Catherine Neven, Wim Huisman, Peter van Delft, Margreet Bakker-Verweij, Sandra G.J. Arkesteijn, Cornelis L. Harteveld & Piero C. Giordano. (2010) Hb St. Truiden [α68(E17)Asn→His] and Hb Westeinde [α125(H8)Leu→Gln]: Two New Abnormalities of the α2-Globin Gene. Hemoglobin 34:5, pages 439-444.
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Cornelis L. Harteveld, Florens G.A. Versteegh, Eduard H.G. van Leer, Jaap S. Starreveld, Peter J.M.J. Kok, Irene van Rooijen-Nijdam, Peter van Delft, Isabelle Zanella-Cleon, Michel Becchi, Henri Wajcman & Piero C. Giordano. (2007) Hb St. Jozef, A Val→Leu N-Terminal Mutation Leading to Retention of the Methionine, and Partial Acetylation Found in the Globin Gene in Cis with a −α3.7 Thalassemia Deletion. Hemoglobin 31:3, pages 313-323.
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Lynda Walker, Barry Eng, Andrew McFarlane & John S. Waye. (2007) High Oxygen Affinity Hemoglobin Variant in a Canadian Family: Hb Bunbury [β94(FG1)Asp→Asn, GAC→AAC]. Hemoglobin 31:1, pages 101-103.
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