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Severe hereditary haemolytic anaemia in a Caucasian newborn: a new fetal haemoglobin variant Hb F-Bonheiden ((G)gamma 38(C4) Thr-->Pro)
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Published in: | European journal of pediatrics 2005-04, Vol.164 (4), p.261-262 |
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Language: | English |
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container_end_page | 262 |
container_issue | 4 |
container_start_page | 261 |
container_title | European journal of pediatrics |
container_volume | 164 |
creator | Van den Driessche, Marleen Moerman, Jan Moens, Marc Van Eldere, Stefaan Derclaye, Isabelle Philippe, Marianne |
description | |
doi_str_mv | 10.1007/s00431-004-1614-7 |
format | article |
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ispartof | European journal of pediatrics, 2005-04, Vol.164 (4), p.261-262 |
issn | 0340-6199 |
language | eng |
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source | Springer Nature |
subjects | Anemia, Hemolytic, Congenital - genetics Humans Infant, Newborn Male Mutation Pedigree |
title | Severe hereditary haemolytic anaemia in a Caucasian newborn: a new fetal haemoglobin variant Hb F-Bonheiden ((G)gamma 38(C4) Thr-->Pro) |
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