Familial differences in the proportion of abnormal hemoglobin present in the sickle cell trait
about
STUDIES OF IN VITRO SYNTHESIS OF HETEROGENIC HEMOGLOBINS.Hypocatalasemia: a new genetic carrier state.Age trends in the prevalence of the sickle cell trait.Qualitative and quantitative control of adult hemoglobin synthesis; a multiple allele hypothesis.Electrophoretic components of the hemoglobin of red cell membranes.QUANTITATIVE STUDIES ON A2, SICKLE CELL, AND FETAL HEMOGLOBINS IN NEGROES WITH MONGOLISM, WITH OBSERVATIONS ON TRANSLOCATION MONGOLISM IN NEGROESSickle-cell Anaemia.
P2860
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P2860
Familial differences in the proportion of abnormal hemoglobin present in the sickle cell trait
description
1951 nî lūn-bûn
@nan
1951 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1951 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1951年の論文
@ja
1951年論文
@yue
1951年論文
@zh-hant
1951年論文
@zh-hk
1951年論文
@zh-mo
1951年論文
@zh-tw
1951年论文
@wuu
name
Familial differences in the pr ...... esent in the sickle cell trait
@ast
Familial differences in the pr ...... esent in the sickle cell trait
@en
type
label
Familial differences in the pr ...... esent in the sickle cell trait
@ast
Familial differences in the pr ...... esent in the sickle cell trait
@en
prefLabel
Familial differences in the pr ...... esent in the sickle cell trait
@ast
Familial differences in the pr ...... esent in the sickle cell trait
@en
P2093
P2860
P356
P1476
Familial differences in the pr ...... esent in the sickle cell trait
@en
P2093
P2860
P304
P356
10.1172/JCI102532
P407
P577
1951-10-01T00:00:00Z