Alpha thalassaemia in British people.

Author:

Higgs D R,Ayyub H,Clegg J B,Hill A V,Nicholls R D,Teal H,Wainscoat J S,Weatherall D J

Publisher

BMJ

Subject

General Earth and Planetary Sciences,General Environmental Science,General Engineering

Reference23 articles.

1. The thalassaemia syndromes;Weatherall, D.J.; Clegg, J.B.,1981

2. Localisation of the human x globin structural gene to chromosome 16 in somatic cell hybrids by molecular hybridisation assay;Deisseroth, A.; Nienhuis, A.; Turner, P.;Cell,1977

3. The chromosomal arrangement of human t-like genes: sequence homology and oc globin gene deletions;Lauer, J.; Shen, C.-K.J.; Maniatis, T.;Cell,1980

4. Alpha thalassemia;Higgs, D.R.; Weatherall, D.J.,1983

5. Abnormal foetal haemoglobins;Silvestroni, E.; Bianco, I.;Nature

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1. α0-Thalassemia Due to a 90.7 kb Deletion (– –NFLD);Hemoglobin;2017-05-04

2. α-thalassaemia;Orphanet Journal of Rare Diseases;2010-05-28

3. Characterisation of the British α0-thalassaemia deletion: evidence of a founder effect in Newfoundland, Canada;British Journal of Haematology;2009-10

4. Leftward ?????4.2 Deletion Alpha-Thalassemia in a Patient of Northern European Extraction;Journal of Pediatric Hematology/Oncology;2004-01

5. 2 α-Thalassaemia;Baillière's Clinical Haematology;1998-03

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