MOLECULAR PATHOLOGY OF CONGENITAL ADRENAL-HYPERPLASIA

被引：22

作者：

STRACHAN, T

机构：

[1] University Department of Medical Genetics, St. Mary's Hospital, Manchester, M13 OJH, Hathersage Road

来源：

CLINICAL ENDOCRINOLOGY | 1990年 / 32卷 / 03期

关键词：

D O I：

10.1111/j.1365-2265.1990.tb00878.x

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：373 / 393

页数：21

共 63 条

[1] DNA AND RNA ANALYSIS OF CYTOCHROME-P-450 21-HYDROXYLASE - TRANSCRIPTIONAL ACTIVITY IN CONGENITAL ADRENAL-HYPERPLASIA [J].

ALOTHMAN, AN ;

DOCHERTY, K ;

MAKGOBA, MW ;

SHEPPARD, MC ;

LONDON, DR .

JOURNAL OF MOLECULAR ENDOCRINOLOGY, 1988, 1 (03) :157-164

[2] MUTATION IN THE CYP21B GENE (ILE-172-]ASN) CAUSES STEROID 21-HYDROXYLASE DEFICIENCY [J].

AMOR, M ;

PARKER, KL ;

GLOBERMAN, H ;

NEW, MI ;

WHITE, PC .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (05) :1600-1604

[3]

BELT KT, 1985, IMMUNOGENETICS, V21, P173

[4] DNA METHYLATION AND THE FREQUENCY OF CPG IN ANIMAL DNA [J].

BIRD, AP .

NUCLEIC ACIDS RESEARCH, 1980, 8 (07) :1499-1504

[5] MAPPING OF STEROID 21-HYDROXYLASE GENES ADJACENT TO COMPLEMENT COMPONENT C-4 GENES IN HLA, THE MAJOR HISTOCOMPATIBILITY COMPLEX IN MAN [J].

CARROLL, MC ;

CAMPBELL, RD ;

PORTER, RR .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (02) :521-525

[6] STRUCTURE AND ORGANIZATION OF THE C4-GENES [J].

CARROLL, MC ;

BELT, T ;

PALSDOTTIR, A ;

PORTER, RR .

PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1984, 306 (1129) :379-388

[7] ADRENAL-STEROIDS IN MATERNAL AND CORD BLOOD AFTER DEXAMETHASONE ADMINISTRATION AT MIDTERM [J].

CHARNVISES, S ;

FENCL, MD ;

OSATHANONDH, R ;

ZHU, MG ;

UNDERWOOD, R ;

TULCHINSKY, D .

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1985, 61 (06) :1220-1222

[8] PULSED FIELD GEL-ELECTROPHORESIS IDENTIFIES A HIGH DEGREE OF VARIABILITY IN THE NUMBER OF TANDEM 21-HYDROXYLASE AND COMPLEMENT C-4 GENE REPEATS IN 21-HYDROXYLASE DEFICIENCY HAPLOTYPES [J].

COLLIER, S ;

SINNOTT, PJ ;

DYER, PA ;

PRICE, DA ;

HARRIS, R ;

STRACHAN, T .

EMBO JOURNAL, 1989, 8 (05) :1393-1402

[9] PRENATAL TREATMENT OF CONGENITAL ADRENAL-HYPERPLASIA RESULTING FROM 21-HYDROXYLASE DEFICIENCY [J].

DAVID, M ;

FOREST, MG .

JOURNAL OF PEDIATRICS, 1984, 105 (05) :799-803

[10]

DAWKINS RL, 1987, J IMMUNOGENET, V14, P89

← 1 2 3 4 5 6 7 →