DELETION OF BETA-GLOBIN STRUCTURE GENE IN HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN

被引：76

作者：

KAN, YW

HOLLAND, JP

DOZY, AM

CHARACHE, S

KAZAZIAN, HH

机构：

[1] UNIV CALIF,SAN FRANCISCO GEN HOSP,SAN FRANCISCO,CA 94110

[2] JOHNS HOPKINS UNIV,SCH MED,BALTIMORE,MD 21205

来源：

NATURE | 1975年 / 258卷 / 5531期

关键词：

D O I：

10.1038/258162a0

中图分类号：

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 ;

摘要：

引用

页码：162 / 163

页数：2

共 11 条

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[4] HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN - HETEROGENEITY OF FETAL HEMOGLOBIN IN HOMOZYGOTES AND IN CONJUNCTION WITH BETA-THALASSEMIA
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[6] A GHANAIAN ADULT, HOMOZYGOUS FOR HEREDITARY PERSISTENCE OF FOETAL HAEMOGLOBIN AND HETEROZYGOUS FOR ELLIPTOCYTOSIS
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[7] DUPLICATION OF STRUCTURAL GENES FOR HEMOGLOBIN ALPHA-CHAINS AND BETA-CHAINS IN MAN
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[J]. ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1974, 241 (NOV29) : 80 - 92
[8] AN ADULT HOMOZYGOUS FOR PERSISTENT FETAL HEMOGLOBIN
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[J]. ANNALS OF INTERNAL MEDICINE, 1970, 72 (04) : 533 - +
[9] HOMOZYGOTE FOR HBGAMMA TYPE OF FETAL HEMOGLOBIN IN INDIA - STUDY OF TWO INDIAN AND FOUR NEGRO FAMILIES
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[J]. BRITISH JOURNAL OF HAEMATOLOGY, 1972, 23 (04) : 403 - +
[10] GENE DELETION AS CAUSE OF ALPHA THALASSEMIA - GENETIC LESION IN HOMOZYGOUS ALPHA THALASSEMIA (HYDROPS FETALIS)
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[J]. NATURE, 1974, 251 (5474) : 392 - 393

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