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Severe hereditary haemolytic anaemia in a Caucasian newborn: A new fetal haemoglobin variant Hb F-Bonheiden (Gγ 38(C4) Thr → Pro)
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Document type | Article de périodique (Journal article) – Article de recherche |
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Access type | Accès restreint |
Publication date | 2005 |
Language | Anglais |
Journal information | "European Journal of Pediatrics" - Vol. 164, no. 4, p. 261-262 (2005) |
Peer reviewed | yes |
issn | 0340-6199 |
Publication status | Publié |
Affiliation | UCL - (SLuc) Service de biochimie médicale |
Links |
- Bain JB (2001) Haemoglobinopathy diagnosis. Blackwell Science, Oxford
- Blouquit Y, Delanoe-Garin J, Lacombe C, Arous N, Cayre Y, Peduzzu J, Braconnier F, Galacteros F (1984) Structural study of hemoglobin Hazebrouck, ?38 (C4) Thr?Pro, a new abnormal hemoglobin with instability and low oxygen affinity. FEBS Lett 172: 155?158
- Coleman MB, Steinber MH, Adams JG (1991) A four-base deletion 5? to the A gamma globin gene is a common polymorphism. Blood 78: 2473?2474
- Kohli-Kumar M, Zwerdling T, Rucknagel DL (1995) Hemoglobin F-Cinncinnati, ?2G?2(41)(C7) Phe?Ser, in a newborn with cyanosis. Am J Hematol 49: 43?47
- Lee-Potter JP, Deacon-Smith RA, Simpkiss MJ, Kamuzora H, Lehmann H (1975) A new cause of haemolytic anaemia in the newborn. A description of an unstable fetal haemoglobin: F Poole, ?2-G?2 130 tryptophan?glycine. J Clin Path 28: 317?320
Bibliographic reference | Van Den Driessche, Marleen ; Moerman, Jan ; Moens, Marc ; Van Eldere, Stefaan ; Derclay, Isabelle ; et. al. Severe hereditary haemolytic anaemia in a Caucasian newborn: A new fetal haemoglobin variant Hb F-Bonheiden (Gγ 38(C4) Thr → Pro). In: European Journal of Pediatrics, Vol. 164, no. 4, p. 261-262 (2005) |
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Permanent URL | http://hdl.handle.net/2078.1/164622 |