HB S-HB Monroe; a sickle cell-beta-thalassemia syndrome.

Tytuł:: HB S-HB Monroe; a sickle cell-beta-thalassemia syndrome.
Autorzy:: Sweeting I; Medical Research Council Laboratories (Jamaica), University of the West Indies, Mona, Kingston.
Serjeant BE
Serjeant GR
Kulozik AE
Vetter B
Źródło:: Hemoglobin [Hemoglobin] 1998 Mar; Vol. 22 (2), pp. 153-6.
Typ publikacji:: Journal Article
Język:: English
Imprint Name(s):: Publication: London : Informa Healthcare
Original Publication: New York, Dekker.
MeSH Terms:: Globins/*genetics
Hemoglobin, Sickle/*analysis
Hemoglobins, Abnormal/*analysis
Sickle Cell Trait/*genetics
beta-Thalassemia/*genetics
Adolescent ; Adult ; Black People/genetics ; Blood Protein Electrophoresis ; Child ; Chromatography, High Pressure Liquid ; Codon/genetics ; Female ; Hemoglobin, Sickle/genetics ; Hemoglobins, Abnormal/genetics ; Heterozygote ; Humans ; Isoelectric Focusing ; Jamaica/epidemiology ; Male ; Sickle Cell Trait/complications ; beta-Thalassemia/complications
Substance Nomenclature:: 0 (Codon)
0 (Hemoglobin, Sickle)
0 (Hemoglobins, Abnormal)
119822-87-6 (hemoglobin Monroe)
9004-22-2 (Globins)
Entry Date(s):: Date Created: 19980512 Date Completed: 19980708 Latest Revision: 20221207
Update Code:: 20240104
DOI:: 10.3109/03630269809092139
PMID:: 9576332
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