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Literature DB >> 19378

Further modification of the microchromatographic determination of hemoglobin A2.

C T Schleider, S M Mayson, T H Huisman.

Abstract

Mesh：

Substances：
Hemoglobins
Hemoglobin A

Year: 1977 PMID： 19378 DOI： 10.3109/03630267709027867

Source DB: PubMed Journal: Hemoglobin ISSN： 0363-0269 Impact factor: 0.849

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Cited

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8 in total

1. Compound heterozygosity for a beta zero-thalassemia (frameshift codons 38/39; -C) and a nondeletional Swiss type of HPFH (A----C at NT -110, G gamma) in a Czechoslovakian family.

Authors: K Indrak; J Indrakova; F Kutlar; D Pospisilova; I Sulovska; E Baysal; T H Huisman
Journal: Ann Hematol Date: 1991-08 Impact factor: 3.673

2. Interaction of heterozygous beta (0)-thalassemia and triplicated alpha globin loci in a Swiss-Spanish family.

Authors: P Beris; R Darbellay; A Hochmann; E Pradervand; P Pugin
Journal: Klin Wochenschr Date: 1991-10-02

3. The frequency of the gamma chain variant A gamma T in different populations, and its use in evaluating gamma gene expression in association with thalassemia.

Authors: T H Huisman; F Kutlar; T Nakatsuji; A Bruce-Tagoe; Y Kilinç; M N Cauchi; C Romero Garcia
Journal: Hum Genet Date: 1985 Impact factor: 4.132

4. Beta S haplotypes in various world populations.

Authors: C Oner; A J Dimovski; N F Olivieri; G Schiliro; J F Codrington; S Fattoum; A D Adekile; R Oner; G T Yüregir; C Altay
Journal: Hum Genet Date: 1992-04 Impact factor: 4.132

5. The in vivo expression of the globin genes of the beta cistron in gamma-, delta-, and delta beta-thalassemia heterozygotes.

Authors: A J Dimovski; A D Adekile; T H Huisman
Journal: Experientia Date: 1994-02-15

Further modification of the microchromatographic determination of hemoglobin A2.

1. Compound heterozygosity for a beta zero-thalassemia (frameshift codons 38/39; -C) and a nondeletional Swiss type of HPFH (A----C at NT -110, G gamma) in a Czechoslovakian family.

2. Interaction of heterozygous beta (0)-thalassemia and triplicated alpha globin loci in a Swiss-Spanish family.

3. The frequency of the gamma chain variant A gamma T in different populations, and its use in evaluating gamma gene expression in association with thalassemia.

4. Beta S haplotypes in various world populations.

5. The in vivo expression of the globin genes of the beta cistron in gamma-, delta-, and delta beta-thalassemia heterozygotes.

6. The levels of zeta, gamma, and delta chains in patients with Hb H disease.

7. Molecular characterization of beta-thalassemia in Czechoslovakia.

8. Prevalence and Genetic Analysis of α- and β-Thalassemia and Sickle Cell Anemia in Southwest Iran.