Clinical Expression of a Rare β-Globin Gene Mutation Co-Inherited with Haemoglobin E-Disease

Wouter W. van Solinge; Bent Lind; Richard van Wijk; Herman Ch. Hart; Rob J. Kraaijenhagen

doi:10.1515/cclm.1996.34.12.949

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Clinical Expression of a Rare β-Globin Gene Mutation Co-Inherited with Haemoglobin E-Disease

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Clinical Chemistry and Laboratory Medicine (CCLM)

From the journal Volume 34 Issue 12

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van Solinge, Wouter W., Lind, Bent, van Wijk, Richard, Hart, Herman Ch. and Kraaijenhagen, Rob J.. "Clinical Expression of a Rare β-Globin Gene Mutation Co-Inherited with Haemoglobin E-Disease" Clinical Chemistry and Laboratory Medicine (CCLM), vol. 34, no. 12, 1996, pp. 949-954. https://doi.org/10.1515/cclm.1996.34.12.949

van Solinge, W., Lind, B., van Wijk, R., Hart, H. & Kraaijenhagen, R. (1996). Clinical Expression of a Rare β-Globin Gene Mutation Co-Inherited with Haemoglobin E-Disease. Clinical Chemistry and Laboratory Medicine (CCLM), 34(12), 949-954. https://doi.org/10.1515/cclm.1996.34.12.949

van Solinge, W., Lind, B., van Wijk, R., Hart, H. and Kraaijenhagen, R. (1996) Clinical Expression of a Rare β-Globin Gene Mutation Co-Inherited with Haemoglobin E-Disease. Clinical Chemistry and Laboratory Medicine (CCLM), Vol. 34 (Issue 12), pp. 949-954. https://doi.org/10.1515/cclm.1996.34.12.949

van Solinge, Wouter W., Lind, Bent, van Wijk, Richard, Hart, Herman Ch. and Kraaijenhagen, Rob J.. "Clinical Expression of a Rare β-Globin Gene Mutation Co-Inherited with Haemoglobin E-Disease" Clinical Chemistry and Laboratory Medicine (CCLM) 34, no. 12 (1996): 949-954. https://doi.org/10.1515/cclm.1996.34.12.949

van Solinge W, Lind B, van Wijk R, Hart H, Kraaijenhagen R. Clinical Expression of a Rare β-Globin Gene Mutation Co-Inherited with Haemoglobin E-Disease. Clinical Chemistry and Laboratory Medicine (CCLM). 1996;34(12): 949-954. https://doi.org/10.1515/cclm.1996.34.12.949

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Published Online: 2009-10-21

Published in Print: 1996

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Articles in the same Issue

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Review
Clinical Expression of a Rare β-Globin Gene Mutation Co-Inherited with Haemoglobin E-Disease
Fast Amplification of the Low Density Lipoprotein Receptor Gene and Detection of a Large Deletion by Means of Long Polymerase Chain Reaction
Age-Dependent Variations of Lactate Dehydrogenase and Creatine Kinase Activities in Water Buffalo Calf Serum
γ-Glutamyltransferase and Serum Proteins in Buffalo Calves Following Colostral Ingestion
Determination of Adenosine Phosphates in Whole Blood by Capillary Zone Electrophoresis
TECHNICAL NOTE
LETTER TO THE EDITOR
Technical Report
Acknowledgement

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https://doi.org/10.1515/cclm.1996.34.12.949

Articles in the same Issue

Titelei
Review
Clinical Expression of a Rare β-Globin Gene Mutation Co-Inherited with Haemoglobin E-Disease
Fast Amplification of the Low Density Lipoprotein Receptor Gene and Detection of a Large Deletion by Means of Long Polymerase Chain Reaction
Age-Dependent Variations of Lactate Dehydrogenase and Creatine Kinase Activities in Water Buffalo Calf Serum
γ-Glutamyltransferase and Serum Proteins in Buffalo Calves Following Colostral Ingestion
Determination of Adenosine Phosphates in Whole Blood by Capillary Zone Electrophoresis
TECHNICAL NOTE
LETTER TO THE EDITOR
Technical Report
Acknowledgement