A Plea for the Newborn Diagnosis of Hb S-Hereditary Persistence of Fetal Hemoglobin

Graham R. SerjeantSickle Cell Trust (Jamaica), Kingston, Jamaica; Correspondence[email protected]
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Beryl E. SerjeantSickle Cell Trust (Jamaica), Kingston, Jamaica; View further author information

Ian R. HambletonCaribbean Institute for Health Research-Chronic Disease Research Centre, University of the West Indies, Barbados, West Indies; View further author information

Matthew OakleyKing’s College London, 1st Floor Cheyne Wing, King’s College Hospital, London, UK; View further author information

Swee Lay TheinSickle Cell Branch, National Heart, Lung and Blood Institute, Bethesda, MD, USAView further author information

Barnaby ClarkKing’s College London, 1st Floor Cheyne Wing, King’s College Hospital, London, UK; View further author information

References

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Serjeant GR, Serjeant BE, Forbes M, et al. Haemoglobin gene frequencies in the Jamaican population: a study of 100,000 newborns. Br J Haematol. 1986;64(2):253–262.
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Saint-Martin C, Romana M, Bibrac A, et al. Universal newborn screening for haemoglobinopathies in Guadeloupe (French West Indies): A 27-year experience. J Med Screen. 2013;20(4):177–182.
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Mason K, Gibson F, Higgs D, et al. Haemoglobin variant screening in Jamaica: Meeting student’s request. Br J Haematol. 2016:172(4):634–636.
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A Plea for the Newborn Diagnosis of Hb S-Hereditary Persistence of Fetal Hemoglobin

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A Plea for the Newborn Diagnosis of Hb S-Hereditary Persistence of Fetal Hemoglobin

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