Genetic influences on F cells and other hematologic variables: a twin heritability study

C. Garner, Thanusak Tatu, Joyce E. Reittie, +7

Blood

Genetic influences on F cells and other hematologic variables: a twin heritability study

C. Garner, Thanusak Tatu, Joyce E. Reittie, +7

Blood

Analysis of the human alpha-globin gene cluster reveals a highly informative genetic locus.

Douglas R. Higgs, James S. Wainscoat, Jonathan Flint, +7

Proceedings of the National Academy of Sciences

GeneticsHuman PolymorphismPathologyMolecular GeneticsGenomics +18

Association between hemolysis and albuminuria in adults with sickle cell anemia

Thomas G. Day, Emma Drašar, Tony Fulford, +2

Haematologica

Glomerular DiseaseImmunohematologyRenal PathologyHemolysis-associated VasculopathyGlomerulonephritis +16

Melanesians and Polynesians share a unique alpha-thalassemia mutation.

Adrian V. S. Hill, D. K. Bowden, R J Trent, +6

PubMed

Recombination within the human embryonic ζ-globin locus: A common ζ-ζ chromosome produced by gene conversion of the ψζ gene

Adrian V. S. Hill, Robert D. Nicholls, S L Thein, +1

Cell

Chromosome DynamicsDevelopmental BiologyCommon ζ-ζ ChromosomeGenetic DisorderGenetics +12

Multiple origins of the sickle mutation: evidence from beta S globin gene cluster polymorphisms.

J. S. Wainscoat, S L Thein, G R Sarjeant, +1

Oxford University Research Archive (ORA) (University of Oxford)

Sickle MutationGeneticsGenetic EpidemiologyHuman PolymorphismPathology +18

Antithrombin Budapest 3 An antithrombin variant with reduced heparin affinity resulting from the substitution L99F

R.J. Olds, David A. Lane, M Boisclair, +3

FEBS Letters

A base substitution (T→C) in codon 29 of the α2‐globin gene causes α thalassaemia

Georgina Hall, S L Thein, Adrian C. Newland, +5

British Journal of Haematology

Homozygous Antithrombin Deficiency: Report of Two New Cases (99 Leu to Phe) Associated with Arterial and Venous Thrombosis

Vijoy Chowdhury, David A. Lane, B Mille, +5

Thrombosis and Haemostasis