Severe hereditary haemolytic anaemia in a Caucasian newborn: A new fetal haemoglobin variant Hb F-Bonheiden (Gγ 38(C4) Thr → Pro)
(2005) European Journal of Pediatrics — Vol. 164, n° 4, p. 261-262 (2005)
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Van Den Driessche, M., Moerman, J., Moens, M., Van Eldere, S., Derclay, I., & Philippe, M. (2005). Severe hereditary haemolytic anaemia in a Caucasian newborn: A new fetal haemoglobin variant Hb F-Bonheiden (Gγ 38(C4) Thr → Pro). European Journal of Pediatrics, 164(4), 261-262. https://doi.org/10.1007/s00431-004-1614-7 (Original work published 2005)