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Article

Hemoglobin Chesterfield (beta 28 Leu----Arg) produces the phenotype of inclusion body beta thalassemia.

Blood - 15 Jun 1991

Thein S L, Best S, Sharpe J, Paul B, Clark D J, Brown M J

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Share to Hemoglobins, Abnormal
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Polymorphism, Restriction Fragment Length

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PMID: 1675132

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Hemoglobin Chesterfield (beta 28 Leu----Arg) produces the phenotype of inclusion body beta thalassemia.PMID 1675132Read ↗

A deletion of 11 bp (CD 131-134) in exon 3 of the beta-globin gene produces the phenotype of inclusion body beta-thalassemia.Semantic proximity Read ↗

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Hemoglobin Hagley Park: a novel (alpha82Ala-->Thr) substitution identified in an infant with severe hemolytic anemia.Semantic proximity Read ↗

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Hb Camperdown [alpha 2 beta 2 104(G6)Arg-->Ser] identified by DNA analysis in a Brazilian family.Semantic proximity Read ↗

Sideroblastic anemia, iron overload, and ALAS2 R452S in African-American males: phenotype and genotype features of five unrelated patients.Semantic proximity Read ↗

Hb Castilla [beta32(B14)Leu --> Arg] caused by a de novo mutation.Semantic proximity Read ↗

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The -87 (C----A) beta(+)-thalassemia mutation in a black family.Semantic proximity Read ↗

Novel hemoglobin (Hb Grey Lynn) substitution (alpha91Leu --> Phe) affects heme interactions and alpha1beta2 contacts.Semantic proximity Read ↗

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