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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
- Correspondence to Dr Roshan B Colah, Scientist F, National Institute of Immunohaematology (Indian Council of Medical Research), 13th floor, New Multistoried Building, K.E.M. Hospital Campus, Parel, Mumbai 400012, India; colahrb{at}gmail.com
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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
Publication history
- Accepted February 29, 2012
- First published March 29, 2012.
Online issue publication
July 07, 2020
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© 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.