Hemoglobinopathies Observed in the Population of the Southeastern United States (SE-USA)

T. H. J. Huisman Comprehensive Sickle Cell Center and Laboratory of Protein Chemistry Department of Cell and Molecular Biology, Medical College of Georgia Augusta, GA, 30912, USA

B. L. Abraham Comprehensive Sickle Cell Center and Laboratory of Protein Chemistry Department of Cell and Molecular Biology, Medical College of Georgia Augusta, GA, 30912, USA

H. F. Harris Comprehensive Sickle Cell Center and Laboratory of Protein Chemistry Department of Cell and Molecular Biology, Medical College of Georgia Augusta, GA, 30912, USA

M. E. Gravely Comprehensive Sickle Cell Center and Laboratory of Protein Chemistry Department of Cell and Molecular Biology, Medical College of Georgia Augusta, GA, 30912, USA

J. Henson Comprehensive Sickle Cell Center and Laboratory of Protein Chemistry Department of Cell and Molecular Biology, Medical College of Georgia Augusta, GA, 30912, USA

D. Williams Comprehensive Sickle Cell Center and Laboratory of Protein Chemistry Department of Cell and Molecular Biology, Medical College of Georgia Augusta, GA, 30912, USA

J. B. Wilson Comprehensive Sickle Cell Center and Laboratory of Protein Chemistry Department of Cell and Molecular Biology, Medical College of Georgia Augusta, GA, 30912, USA

A. Miller Comprehensive Sickle Cell Center and Laboratory of Protein Chemistry Department of Cell and Molecular Biology, Medical College of Georgia Augusta, GA, 30912, USA

S. Mayson Comprehensive Sickle Cell Center and Laboratory of Protein Chemistry Department of Cell and Molecular Biology, Medical College of Georgia Augusta, GA, 30912, USA

R. N. Wrightstone Comprehensive Sickle Cell Center and Laboratory of Protein Chemistry Department of Cell and Molecular Biology, Medical College of Georgia Augusta, GA, 30912, USA

E. Moss Comprehensive Sickle Cell Center and Laboratory of Protein Chemistry Department of Cell and Molecular Biology, Medical College of Georgia Augusta, GA, 30912, USA

B. Joseph Comprehensive Sickle Cell Center and Laboratory of Protein Chemistry Department of Cell and Molecular Biology, Medical College of Georgia Augusta, GA, 30912, USA

L. Walker Comprehensive Sickle Cell Center and Laboratory of Protein Chemistry Department of Cell and Molecular Biology, Medical College of Georgia Augusta, GA, 30912, USA

J. Brisco Comprehensive Sickle Cell Center and Laboratory of Protein Chemistry Department of Cell and Molecular Biology, Medical College of Georgia Augusta, GA, 30912, USA

L. Brisco Comprehensive Sickle Cell Center and Laboratory of Protein Chemistry Department of Cell and Molecular Biology, Medical College of Georgia Augusta, GA, 30912, USA

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Abstract

A survey of nearly 250,000 citizens of Georgia and South Carolina conducted during the past twenty years has led to the detection of over 40 abnormal hemoglobins and several additional he-moglobinopathies. The presence of some of these hemoglobin abnormalities cause (severe) clinical symptoms but others remain undetected unless a specific search is initiated.

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Hemoglobinopathies Observed in the Population of the Southeastern United States (SE-USA)

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Hemoglobinopathies Observed in the Population of the Southeastern United States (SE-USA)

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