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Nontransfusional Iron Overload in Thalassemia: Association with Hereditary Hemochromatosis.
- Published in:
- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 490, doi. 10.1111/j.1749-6632.1998.tb10530.x
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- Article
Phenotypic Prediction in β-Thalassemia.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 436, doi. 10.1111/j.1749-6632.1998.tb10514.x
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- Article
Hb questembert is due to a base substitution (T→C) in codon 131 of the α 2-globin gene and has an α-thalassemia biosynthetic ratio.
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- American Journal of Hematology, 1995, v. 48, n. 4, p. 289, doi. 10.1002/ajh.2830480419
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- Article
Secondary treatment of polycythemia rubra vera with 6-thioguanine.
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- 1982
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- Publication type:
- journal article
Identical twin marrow transplantation for 5 patients with chronic myeloid leukaemia: Role of DNA finger-printing to confirm monozygosity in 3 cases.
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- European Journal of Haematology, 1987, v. 39, n. 2, p. 144, doi. 10.1111/j.1600-0609.1987.tb00744.x
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- Publication type:
- Article
Interaction Between Two Quantitative Trait Loci Affects Fetal Haemoglobin Expression.
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- Annals of Human Genetics, 2005, v. 69, n. 6, p. 707, doi. 10.1111/j.1529-8817.2005.00188.x
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- Publication type:
- Article
Detection of fetal cells in maternal blood.
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- Prenatal Diagnosis, 1991, v. 11, n. 2, p. 117, doi. 10.1002/pd.1970110207
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- Article
Evolutionary relationships of human populations.
- Published in:
- Nature, 1986, v. 323, n. 6090, p. 744, doi. 10.1038/323744c0
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- Article
Ha-ras hypervariable alleles in myelodysplasia.
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- Nature, 1986, v. 321, n. 6065, p. 84, doi. 10.1038/321084a0
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- Publication type:
- Article
Evolutionary relationships of human populations from an analysis of nuclear DNA polymorphisms.
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- Nature, 1986, v. 319, n. 6053, p. 491, doi. 10.1038/319491a0
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- Publication type:
- Article
Individual-specific 'fingerprints' of human DNA.
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- Nature, 1985, v. 316, n. 6023, p. 76, doi. 10.1038/316076a0
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- Publication type:
- Article
Peak expiratory flow in Afro-Caribbean children with and without sickle cell anaemia.
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- Acta Paediatrica, 2007, v. 96, n. 9, p. 1308, doi. 10.1111/j.1651-2227.2007.00411.x
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- Publication type:
- Article
Next-generation sequencing as a tool for breakpoint analysis in rearrangements of the globin gene clusters.
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- International Journal of Laboratory Hematology, 2017, v. 39, p. 111, doi. 10.1111/ijlh.12680
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- Publication type:
- Article
A Novel Deletion in the β-Globin Gene Complex.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 20, doi. 10.1111/j.1749-6632.1985.tb17171.x
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- Publication type:
- Article
Genetic and Molecular Analysis of Mild Forms of Homozygous β-Thalassemia.
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- Annals of the New York Academy of Sciences, 1985, v. 445, n. 1, p. 68, doi. 10.1111/j.1749-6632.1985.tb17176.x
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- Publication type:
- Article
Alpha-thalassaemia trait as a cause of unexplained microcytosis in a South African population.
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- SAMJ: South African Medical Journal, 2016, v. 106, n. 3, p. 276, doi. 10.7196/SAMJ.2016.v106i3.10005
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- Publication type:
- Article
Antithrombins Southport (Leu 99 to Val) and Vienna (Cln 118 to Pro): two novel antithrombin variants with abnormal heparin binding.
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- British Journal of Haematology, 1995, v. 89, n. 3, p. 602, doi. 10.1111/j.1365-2141.1995.tb08369.x
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- Article
Association of a novel high oxygen affinity haemoglobin variant with δβ thalassaemia.
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- British Journal of Haematology, 1994, v. 86, n. 1, p. 118, doi. 10.1111/j.1365-2141.1994.tb03261.x
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- Article
Identification of nine novel mutations in type I antithrombin deficiency by heteroduplex screening.
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- British Journal of Haematology, 1993, v. 84, n. 4, p. 656, doi. 10.1111/j.1365-2141.1993.tb03142.x
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- Article
The molecular basis of HPFH in a British family identified by heteroduplex formation.
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- British Journal of Haematology, 1993, v. 84, n. 1, p. 106, doi. 10.1111/j.1365-2141.1993.tb03032.x
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- Article
Beta thalassaemia in the indigenous British population.
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- British Journal of Haematology, 1992, v. 82, n. 3, p. 584, doi. 10.1111/j.1365-2141.1992.tb06471.x
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- Article
A NOVEL MUTATION (NONSENSE β 127) IN EXON 3 OF THE β GLOBIN GENE PRODUCES A VARIABLE THALASSAEMIC PHENOTYPE.
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- British Journal of Haematology, 1991, v. 79, n. 2, p. 342, doi. 10.1111/j.1365-2141.1991.tb04548.x
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- Article
A simple and rapid method of direct sequencing using Dynabeads.
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- British Journal of Haematology, 1991, v. 79, n. 1, p. 113, doi. 10.1111/j.1365-2141.1991.tb08016.x
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- Article
Antithrombin Glasgow II: alanine 382 to threonine mutation in the serpin P12 position, resulting in a substrate reaction with thrombin.
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- British Journal of Haematology, 1991, v. 79, n. 1, p. 70, doi. 10.1111/j.1365-2141.1991.tb08009.x
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- Article
A SPONTANEOUS DELETION OF β33/34 Val IN EXON 2 OF THE β GLOBIN GENE (Hb KOREA) PRODUCES THE PHENOTYPE OF DOMINANT β THALASSAEMIA.
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- British Journal of Haematology, 1991, v. 78, n. 4, p. 581, doi. 10.1111/j.1365-2141.1991.tb04499.x
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- Article
A novel δº mutation in cis with Hb Knossos: a study of different genetic interactions in three Egyptian families.
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- British Journal of Haematology, 1991, v. 78, n. 3, p. 430, doi. 10.1111/j.1365-2141.1991.tb04460.x
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- Article
Novel point mutations leading to type 1 antithrombin deficiency and thrombosis.
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- British Journal of Haematology, 1991, v. 78, n. 3, p. 408, doi. 10.1111/j.1365-2141.1991.tb04456.x
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- Publication type:
- Article
Antithrombin Vicenza, Ala 384 to Pro (GCA to CCA) mutation, transforming the inhibitor into a substrate.
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- British Journal of Haematology, 1991, v. 77, n. 1, p. 87, doi. 10.1111/j.1365-2141.1991.tb07953.x
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- Article
The molecular basis of thalassaemia major and thalassaemia intermedia in Asian Indians: application to prenatal diagnosis.
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- British Journal of Haematology, 1988, v. 70, n. 2, p. 225, doi. 10.1111/j.1365-2141.1988.tb02468.x
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- Article
Thalassaemia intermedia: interaction of the triple α-globin gene arrangement and heterozygous β-thalassaemia.
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- British Journal of Haematology, 1987, v. 66, n. 1, p. 109, doi. 10.1111/j.1365-2141.1987.00103.x-i1
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- Article
Association of thalassaemia intermedia with a beta-globin gene haplotype.
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- British Journal of Haematology, 1987, v. 65, n. 3, p. 367, doi. 10.1111/j.1365-2141.1987.tb06870.x
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- Article
THE AVA II Ψβ POLYMORPHISM IS LINKED TO THE COMMON MEDITERRANEAN β<sup>+</sup> THALASSAEMIA MUTATION.
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- British Journal of Haematology, 1985, v. 61, n. 4, p. 747, doi. 10.1111/j.1365-2141.1985.tb02889.x
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- Article
A genetic marker for elevated levels of haemoglobin F in homozygous sickle cell disease?
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- British Journal of Haematology, 1985, v. 60, n. 2, p. 261, doi. 10.1111/j.1365-2141.1985.tb07412.x
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- Article
Population and genetic studies suggest a single origin for the Indian deletion β° thalassaemia.
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- British Journal of Haematology, 1984, v. 57, n. 2, p. 271, doi. 10.1111/j.1365-2141.1984.tb02896.x
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- Publication type:
- Article
HAEMATOLOGICAL PHENOTYPE OF THE TRIPLICATED γ-GLOBIN GENE ARRANGEMENT.
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- British Journal of Haematology, 1984, v. 57, n. 2, p. 349, doi. 10.1111/j.1365-2141.1984.tb02904.x
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- Article
Thalassaemia intermedia: a new molecular basis.
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- British Journal of Haematology, 1984, v. 56, n. 2, p. 333, doi. 10.1111/j.1365-2141.1984.tb03960.x
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- Publication type:
- Article
Graft-versus-host disease after treatment for chronic granulocytic leukaemia in transformation.
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- British Journal of Haematology, 1982, v. 52, n. 3, p. 383, doi. 10.1111/j.1365-2141.1982.tb03907.x
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- Publication type:
- Article
Venous thromboembolism in adults with sickle cell disease: experience of a single centre in the UK.
- Published in:
- 2016
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- Publication type:
- journal article