Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Microchromatography of hemoglobins. II. A rapid method for the determination of hemoglobin A2.

× No keyword cloud information.

13 in total

1. A G gamma type of the hereditary persistence of fetal hemoglobin with beta chain production in cis.

Authors: T H Huisman; A Miller; W A Schroeder
Journal: Am J Hum Genet Date: 1975-11 Impact factor: 11.025

2. The chemical heterogeneity of the fetal hemoglobin in normal newborn infants and in adults.

Authors: T H Huisman; H Harris; M Gravely
Journal: Mol Cell Biochem Date: 1977-08-19 Impact factor: 3.396

3. Inheritance of F cell frequency in heterocellular hereditary persistence of fetal hemoglobin: an example of allelic exclusion.

Authors: S H Boyer; L Margolet; M L Boyer; T H Huisman; W A Schroeder; W G Wood; D J Weatherall; J B Clegg; R Cartner
Journal: Am J Hum Genet Date: 1977-05 Impact factor: 11.025

4. One haplotype is associated with the Swiss type of hereditary persistence of fetal hemoglobin in the Yugoslavian population.

Authors: G D Efremov; I Gjorgovski; N Stojanovski; J C Diaz-Chico; T Harano; F Kutlar; T H Huisman
Journal: Hum Genet Date: 1987-10 Impact factor: 4.132

5. Haemoglobin A2 in newborn infants of different maturity.

Authors: P Neumeyer; K Betke
Journal: Eur J Pediatr Date: 1987-11 Impact factor: 3.183

6. Partial mispairing and crossing-over between beta 0 and delta genes as the origin of the delta beta 0 thalassemia gene. A single mutational event hypothesis.

Authors: J M Cantú; B Ibarra; G Vaca; M L Ramirez; J Sánchez-Corona
Journal: Hum Genet Date: 1979-06-19 Impact factor: 4.132

Microchromatography of hemoglobins. II. A rapid method for the determination of hemoglobin A2.

1. A G gamma type of the hereditary persistence of fetal hemoglobin with beta chain production in cis.

2. The chemical heterogeneity of the fetal hemoglobin in normal newborn infants and in adults.

3. Inheritance of F cell frequency in heterocellular hereditary persistence of fetal hemoglobin: an example of allelic exclusion.

4. One haplotype is associated with the Swiss type of hereditary persistence of fetal hemoglobin in the Yugoslavian population.

5. Haemoglobin A2 in newborn infants of different maturity.

6. Partial mispairing and crossing-over between beta 0 and delta genes as the origin of the delta beta 0 thalassemia gene. A single mutational event hypothesis.

7. Proportion of fetal hemoglobin synthesis decreases during erythroid cell maturation.

8. Fetal hemoglobin accumulation in vitro. Effect of adherent mononuclear cells.

9. Hemoglobin Evanston (alpha 14 Trp----Arg). An unstable alpha-chain variant expressed as alpha-thalassemia.

10. Haemoglobin K Woolwich: a study of the family of a homozygote.