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Hemoglobin
international journal for hemoglobin research
Volume 31, 2007 - Issue 3
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Hb Zoetermeer: A New Mutation on the α2 Gene Inducing an Ala→Ser Substitution at Codon 21 is Possibly Associated with a Mild Thalassemic Phenotype

Cornelis L. Harteveld The Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands
,
Willem C.H. van Helden Department of Clinical Chemistry, Lange Land Hospital, Zoetermeer, The Netherlands
,
George L. Boxma General Practitioner, Zoetermeer, The Netherlands
,
Peter van Delft The Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands
,
Margaretha Bakker-Verweij The Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands
,
Henri Wajcman INSERM U654, Créteil, France; Laboratoire de Biochimie, Hôpital Henri Mondor, AP-HP, Créteil, France
,
Isabelle Zanella-Cleon Institut de Biologie et Chimie des Protéines (IFR128), Lyon, France
,
Michel Becchi Institut de Biologie et Chimie des Protéines (IFR128), Lyon, France
&
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 325-332 | Received 04 Sep 2006, Accepted 07 Feb 2007, Published online: 07 Jul 2009

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Carsten W. Lederer, A. Nazli Basak, Yesim Aydinok, Soteroula Christou, Amal El-Beshlawy, Androulla Eleftheriou, Slaheddine Fattoum, Alex E. Felice, Eitan Fibach, Renzo Galanello, Roberto Gambari, Lucian Gavrila, Piero C. Giordano, Frank Grosveld, Helen Hassapopoulou, Eva Hladka, Emmanuel Kanavakis, Franco Locatelli, John Old, George P. Patrinos, Giovanni Romeo, Ali Taher, Joanne Traeger-Synodinos, Panayiotis Vassiliou, Ana Villegas, Ersi Voskaridou, Henri Wajcman, Anastasios Zafeiropoulos & Marina Kleanthous. (2009) An Electronic Infrastructure for Research and Treatment of the Thalassemias and Other Hemoglobinopathies: The Euro-Mediterranean Ithanet Project. Hemoglobin 33:3-4, pages 163-176.
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Stephen O. Brennan, Tim Chan, Sheila Ryken & Anna Ruskova. (2009) A Second Case of Hb Fontainebleau [α21(B2)Ala→Pro] in an Individual with Microcytosis. Hemoglobin 33:3-4, pages 258-261.
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Articles from other publishers (4)

Mariana F. Nery, José Ignacio Arroyo & Juan C. Opazo. (2013) Genomic Organization and Differential Signature of Positive Selection in the Alpha and Beta Globin Gene Clusters in Two Cetacean Species. Genome Biology and Evolution 5:12, pages 2359-2367.
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Dipti S Upadhye, Dipty Jain, Sona B Nair, Anita H Nadkarni, Kanjaksha Ghosh & Roshan B Colah. (2012) First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional α gene variants identified in neonates during newborn screening for sickle cell disorders. Journal of Clinical Pathology 65:7, pages 654-659.
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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 .

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