A NEW VARIANT OF HAEMOGLOBIN A2 AND ITS SEGREGATION IN A FAMILY WITH HAEMOGLOBIN S

被引:35
作者
RANNEY, HM
CORDOVA, FA
BRADLEY, TB
JACOBS, AS
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10.1038/197164a0
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O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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页码:164 / &
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共 15 条
[1]  
BARNABAS J., 1962, NATURE, V194, P931, DOI 10.1038/194931a0
[2]  
CEPPELLINI R, BIOCHEMISTRY HUMAN G, P133
[3]  
FESSAS P, 1962, BLOOD, V19, P1
[4]   A NEW HEREDITARY HEMOGLOBINOPATHY (THE LEPORE TRAIT) AND ITS INTERACTION WITH THALASSEMIA TRAIT [J].
GERALD, PS ;
DIAMOND, LK .
BLOOD, 1958, 13 (09) :835-844
[5]  
GERALD PS, 1961, AM J DIS CHILD, V102, P514
[6]  
GERALD PS, 1961, J BIOL CHEM, V236, P2155
[7]   STUDIES ON AN ABNORMAL MINOR HEMOGLOBIN COMPONENT (HB-B2) [J].
HORTON, B ;
BRIDGES, MT ;
PAYNE, RA ;
HUISMAN, THJ .
CLINICA CHIMICA ACTA, 1961, 6 (02) :246-&
[8]   POLYPEPTIDE CHAINS OF HAEMOGLOBIN-A2 AND HAEMOGLOBIN-G2 [J].
HUEHNS, ER ;
SHOOTER, EM .
JOURNAL OF MOLECULAR BIOLOGY, 1961, 3 (03) :257-&
[9]   THALASSEMIA MINOR ASSOCIATED WITH HEMOGLOBIN-B2 HETEROZYGOSITY - A FAMILY REPORT [J].
HUISMAN, TH ;
PUNT, K ;
SCHAAD, JDG .
BLOOD, 1961, 17 (06) :747-&
[10]   OBSERVATIONS ON THE MINOR BASIC HEMOGLOBIN COMPONENT IN THE BLOOD OF NORMAL INDIVIDUALS AND PATIENTS WITH THALASSEMIA [J].
KUNKEL, HG ;
CEPPELLINI, R ;
MULLEREBERHARD, U ;
WOLF, J .
JOURNAL OF CLINICAL INVESTIGATION, 1957, 36 (11) :1615-1625