THE THALASSEMIA SYNDROMES. BIOCHEMICAL, GENETIC AND CLINICAL CONSIDERATIONS.
作者信息
SIEGAL S
出版信息
Am J Med. 1964 Jun;36:919-35.
PMID:14162897
Abstract
摘要
相似文献
1
THE THALASSEMIA SYNDROMES. BIOCHEMICAL, GENETIC AND CLINICAL CONSIDERATIONS.
Am J Med. 1964 Jun;36:919-35.
2
HEMOGLOBINS A AND F: FORMATION IN THALASSEMIA AND OTHER HEMOLYTIC ANEMIAS.
Science. 1964 May 1;144(3618):552-3. doi: 10.1126/science.144.3618.552.
3
RIBOSOMES ACTIVE IN PROTEIN SYNTHESIS IN HUMAN RETICULOCYTES: A DEFECT IN THALASSEMIA MAJOR.
Nature. 1963 Aug 17;199:706-7. doi: 10.1038/199706a0.
4
[THALASSEMIA. CONTRIBUTION TO THE STUDY OF ITS BIOCHEMICAL HETEROGENEITY IN PORTUGAL].
An Inst Med Trop (Lisb). 1963 Jan-Dec;20:175-312.
5
[ANEMIAS CAUSED BY ABNORMAL HEMOGLOBINS].
Sem Hop. 1964 Apr 20;40:1161-9.
6
7
CONTROL OF PROTEIN SYNTHESIS IN RETICULOCYTES AND THE FORMATION OF HEMOGLOBINS A AND F IN THALAESSMIA SYNDROMES AND OTHER HEMOLYTIC ANEMIAS.
Medicine (Baltimore). 1964 Nov;43:769-78. doi: 10.1097/00005792-196411000-00020.
8
ERYTHROCYTE LIFE-SPAN AND SITES OF DESTRUCTION IN THALASSEMIA MAJOR. RELATION TO CLINICAL AND LABORATORY FINDINGS.
Acta Haematol. 1963;30:204-14. doi: 10.1159/000208125.
9
CONTROLLER-GENE DISEASES: THE OPERON MODEL AS APPLIED TO BETA-THALASSEMIA, FAMILIAL FETAL HEMOGLOBINEMIA AND THE NORMAL SWITCH FROM THE PRODUCTION OF FETAL HEMOGLOBIN TO THAT OF ADULT HEMOGLOBIN.
J Mol Biol. 1964 Jan;8:128-47. doi: 10.1016/s0022-2836(64)80154-6.
10
CASEBOOKS OF THE ABNORMAL GENE. INVESTIGATION OF SOME INBORN METABOLIC ERRORS.
S Afr Med J. 1963 Dec 14;37:1255-61.
引用本文的文献
1
Thalassaemia intermedia: a genetic study in 11 patients.
J Med Genet. 1970 Mar;7(1):47-51. doi: 10.1136/jmg.7.1.47.
Zotero 插件