Literature DB >> 15645283

Severe hereditary haemolytic anaemia in a Caucasian newborn: a new fetal haemoglobin variant Hb F-Bonheiden ((G)gamma 38(C4) Thr-->Pro).

Marleen Van den Driessche1, Jan Moerman, Marc Moens, Stefaan Van Eldere, Isabelle Derclaye, Marianne Philippe.   

Abstract

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Year:  2005        PMID： 15645283     DOI： 10.1007/s00431-004-1614-7

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


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  4 in total

1.  A new cause of haemolytic anaemia in the newborn. A description of an unstable fetal haemoglobin: F Poole, alpha2-G-gamma2 130 trptophan yeilds glycine.

Authors:  J P Lee-Potter; R A Deacon-Smith; M J Simpkiss; H Kamuzora; H Lehmann
Journal:  J Clin Pathol       Date:  1975-04       Impact factor: 3.411

2.  A four-base deletion 5' to the A gamma globin gene is a common polymorphism.

Authors:  M B Coleman; M H Steinberg; J G Adams
Journal:  Blood       Date:  1991-11-01       Impact factor: 22.113

3.  Structural study of hemoglobin Hazebrouck, beta 38(C4)Thr----Pro. A new abnormal hemoglobin with instability and low oxygen affinity.

Authors:  Y Blouquit; J Delanoe-Garin; C Lacombe; N Arous; Y Cayre; J Peduzzi; F Braconnier; F Galacteros
Journal:  FEBS Lett       Date:  1984-07-09       Impact factor: 4.124

4.  Hemoglobin F-Cincinnati, alpha 2G gamma 2 41(C7) Phe-->Ser in a newborn with cyanosis.

Authors:  M Kohli-Kumar; T Zwerdling; D L Rucknagel
Journal:  Am J Hematol       Date:  1995-05       Impact factor: 10.047
  4 in total

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