Alpha thalassaemia in British people.

Alpha thalassaemia in British people.

Although alpha thalassaemia is rare in north Europeans, it has been identified in British people with no known foreign ancestry. Twelve such patients were studied, of whom eight shared a distinctive molecular defect, which was clearly different from defects seen in subjects of Mediterranean or South...

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Príomhchruthaitheoirí:	Higgs, D, Ayyub, H, Clegg, J, Hill, A, Nicholls, R, Teal, H, Wainscoat, J, Weatherall, D
Formáid:	Journal article
Teanga:	English
Foilsithe / Cruthaithe:	1985

Míreanna comhchosúla

α thalassaemia in British people
de réir: Higgs, DR, et al.
Foilsithe / Cruthaithe: (1985)

The alpha thalassaemias.
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THE ALPHA-3.7 AND ALPHA-4.2 DELETION FORMS OF ALPHA+-THALASSAEMIA DIFFER IN SEVERITY
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Alpha-thalassaemia and the malaria hypothesis.
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Molecular rearrangements of the human alpha-globin gene cluster.
de réir: Higgs, D, et al.
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Alpha-thalassaemia caused by a polyadenylation signal mutation.
de réir: Higgs, D, et al.
Foilsithe / Cruthaithe: (1983)

Splenic size in homozygous alpha+ thalassaemia.
de réir: Williams, T, et al.
Foilsithe / Cruthaithe: (1998)

The interaction of alpha thalassaemia and sickle cell-beta zero thalassaemia.
de réir: Vyas, P, et al.
Foilsithe / Cruthaithe: (1988)

Alpha-thalassaemia in Nigeria: Its interaction with sickle-cell disease
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Alpha-thalassaemia.
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Alpha thalassaemia is associated with increased soluble transferrin receptor levels.
de réir: Rees, D, et al.
Foilsithe / Cruthaithe: (1998)

Hb H hydrops fetalis syndrome associated with the interaction of two common determinants of alpha thalassaemia (--MED/(alpha)TSaudi(alpha)).
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Analysis of the human alpha-globin gene cluster reveals a highly informative genetic locus.
de réir: Higgs, D, et al.
Foilsithe / Cruthaithe: (1986)

A newly defined X linked mental retardation syndrome associated with alpha thalassaemia.
de réir: Gibbons, R, et al.
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De novo deletion within the telomeric region flanking the human alpha globin locus as a cause of alpha thalassaemia.
de réir: Viprakasit, V, et al.
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Red blood cell phenotypes in the alpha + thalassaemias from early childhood to maturity.
de réir: Williams, T, et al.
Foilsithe / Cruthaithe: (1996)

High frequency of beta thalassaemia in a small island population in Melanesia.
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Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions.
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Alpha globin genotypes in two North European populations.
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The interaction of alpha thalassaemia with malaria.
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Identification of acquired somatic mutations in the chromatin remodelling factor ATRX in the a thalassaemia myelodysplasia syndrome (ATMDS)
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THE ASSOCIATION OF ALPHA-THALASSEMIA AND MALARIA IN MELANESIA
de réir: Flint, J, et al.
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Alpha thalassaemia mental retardation (ATR-X): an atypical family.
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Thalassaemia.
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Thalassaemia
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Prevalence and molecular basis of alpha-thalassaemia in a malaria endemic region of Vietnam
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Independent recombination events between the duplicated human alpha globin genes; implications for their concerted evolution.
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The non-deletion alpha thalassaemia/mental retardation syndrome: further support for X linkage.
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Thalassaemia in Sri Lanka: implications for the future health burden of Asian populations. Sri Lanka Thalassaemia Study Group.
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Screening of concurrent alpha-Thalassaemia 1 in beta-Thalassaemia carriers
de réir: Chong, Y.M., et al.
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The effect of alpha+-thalassaemia on the incidence of malaria and other diseases in children living on the coast of Kenya.
de réir: Wambua, S, et al.
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Screening of Alpha-Thalassaemia 1 in Beta-Thalassaemia Carriers
de réir: Chong, Yi Min
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Characterization of a new α° thalassaemia defect in the South African population
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Thalassaemia in Sri Lanka: A molecular basis.
de réir: Fisher, C, et al.
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X linked alpha thalassaemia/mental retardation: spectrum of clinical features in three related males.
de réir: Wilkie, A, et al.
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alpha-thalassaemia, X-linked mental retardation syndrome protein, ATRX, interacts with ribosomal genes.
de réir: Law, M, et al.
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Melanesians and Polynesians share a unique alpha-thalassemia mutation.
de réir: Hill, A, et al.
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α-thalassaemia
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Survival and desferrioxamine in thalassaemia major.
de réir: Modell, B, et al.
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