CHARACTERIZATION OF FREQUENT DELETIONS CAUSING STEROID 21-HYDROXYLASE DEFICIENCY

被引：210

作者：

WHITE, PC ^{[1
]}

VITEK, A ^{[1
]}

DUPONT, B ^{[1
]}

NEW, MI ^{[1
]}

机构：

[1] SLOAN KETTERING INST CANC RES,HUMAN IMMUNOGENET LAB,NEW YORK,NY 10021

来源：

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA | 1988年 / 85卷 / 12期

关键词：

D O I：

10.1073/pnas.85.12.4436

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：4436 / 4440

页数：5

共 29 条

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[2]

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[5]

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[6] RESTRICTION MAPS AND RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISMS OF THE HUMAN 21-HYDROXYLASE GENES [J].

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[7]

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[8]

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[9] PHARMACOLOGIC SUPPRESSION OF THE FETAL ADRENAL-GLAND INUTERO - ATTEMPTED PREVENTION OF ABNORMAL EXTERNAL GENITAL MASCULINIZATION IN SUSPECTED CONGENITAL ADRENAL-HYPERPLASIA [J].

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SCHULMAN, JD .

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[10] A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].

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