GENOTYPING STEROID 21-HYDROXYLASE DEFICIENCY - HORMONAL REFERENCE DATA

被引：517

作者：

NEW, MI ^{[1
]}

LORENZEN, F ^{[1
]}

LERNER, AJ ^{[1
]}

KOHN, B ^{[1
]}

OBERFIELD, SE ^{[1
]}

POLLACK, MS ^{[1
]}

DUPONT, B ^{[1
]}

STONER, E ^{[1
]}

LEVY, DJ ^{[1
]}

PANG, S ^{[1
]}

LEVINE, LS ^{[1
]}

机构：

[1] MEM SLOAN KETTERING CANC CTR, HUMAN IMMUNOGENET SECT, NEW YORK, NY 10021 USA

来源：

关键词：

D O I：

10.1210/jcem-57-2-320

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：320 / 326

页数：7

共 41 条

[1] Bartolotta E, 1981, Pediatr Med Chir, V3, P287
[2] ADULT-ONSET FAMILIAL ADRENAL 21-HYDROXYLASE DEFICIENCY
BLANKSTEIN, J
FAIMAN, C
REYES, FI
SCHROEDER, ML
WINTER, JSD
[J]. AMERICAN JOURNAL OF MEDICINE, 1980, 68 (03) : 441 - 448
[3] CONGENITAL ADRENAL-HYPERPLASIA DUE TO PARTIAL 21-HYDROXYLASE DEFICIENCY - A STUDY OF 5 CASES
BOUCHARD, P
KUTTENN, F
MOWSZOWICZ, I
SCHAISON, G
RAUXEURIN, MC
MAUVAISJARVIS, P
[J]. ACTA ENDOCRINOLOGICA, 1981, 96 (01): : 107 - 111
[4] CACCIARI E, 1983, RECENT PROGR PEDIATR, P221
[5] LATE-ONSET 21-HYDROXYLASE DEFICIENCY MIMICKING IDIOPATHIC HIRSUTISM OR POLYCYSTIC OVARIAN DISEASE - AN ALLELIC VARIANT OF CONGENITAL VIRILIZING ADRENAL-HYPERPLASIA WITH A MILDER ENZYMATIC DEFECT
CHROUSOS, GP
LORIAUX, DL
MANN, DL
CUTLER, GB
[J]. ANNALS OF INTERNAL MEDICINE, 1982, 96 (02) : 143 - 148
[6] Danilovs J., 1980, HISTOCOMPATIBILITY T, P287
[7] DAVID R, 1977, CONGENITAL ADRENAL H, P195
[8] DUPONT B, 1977, LANCET, V2, P1309
[9] DUPONT B, 1980, HISTOCOMPATIBILITY T, P693
[10] PLASMA 17-HYDROXYPROGESTERONE, 21-DEOXYCORTISOL AND CORTISOL IN CONGENITAL ADRENAL-HYPERPLASIA
FRANKS, RC
[J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1974, 39 (06) : 1099 - 1102