X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (2754) 2754
Publication (194) 194
Book Chapter (33) 33
Book Review (27) 27
Conference Proceeding (11) 11
Dissertation (6) 6
Magazine Article (2) 2
Book / eBook (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (2073) 2073
female (1472) 1472
21-hydroxylase deficiency (1432) 1432
male (1123) 1123
endocrinology & metabolism (1090) 1090
steroid 21-hydroxylase - genetics (888) 888
congenital adrenal hyperplasia (829) 829
index medicus (790) 790
congenital adrenal-hyperplasia (727) 727
adrenal hyperplasia, congenital - genetics (721) 721
adult (617) 617
child (544) 544
adolescent (509) 509
mutation (456) 456
adrenal hyperplasia, congenital - diagnosis (449) 449
pediatrics (410) 410
genotype (398) 398
diagnosis (384) 384
steroid 21-hydroxylase deficiency (384) 384
infant, newborn (367) 367
child, preschool (364) 364
adrenogenital syndrome (333) 333
phenotype (331) 331
infant (290) 290
pregnancy (274) 274
children (272) 272
genetic disorders (264) 264
adrenal hyperplasia, congenital - complications (262) 262
adrenal hyperplasia, congenital - drug therapy (262) 262
adrenal hyperplasia, congenital - enzymology (256) 256
women (256) 256
mutations (240) 240
steroid 21-hydroxylase (220) 220
steroid 21-hydroxylase - metabolism (220) 220
genetics & heredity (219) 219
gene (212) 212
17-alpha-hydroxyprogesterone - blood (202) 202
alleles (201) 201
hyperplasia (201) 201
adrenal hyperplasia, congenital - physiopathology (187) 187
middle aged (185) 185
polymerase chain reaction (176) 176
animals (173) 173
base sequence (173) 173
deficiency (173) 173
obstetrics & gynecology (173) 173
adrenal hyperplasia, congenital - blood (168) 168
biochemistry & molecular biology (168) 168
molecular sequence data (160) 160
genes (142) 142
haplotypes (142) 142
glucocorticoids - therapeutic use (141) 141
medicine, general & internal (139) 139
pedigree (139) 139
disease (138) 138
prenatal diagnosis (138) 138
17-hydroxyprogesterone (137) 137
adrenal hyperplasia, congenital (136) 136
young adult (135) 135
genetic aspects (132) 132
adrenal hyperplasia, congenital - epidemiology (131) 131
retrospective studies (130) 130
cytochrome p-450 (129) 129
analysis (128) 128
adrenal hyperplasia, congenital - therapy (124) 124
adrenal glands (122) 122
point mutation (122) 122
21-hydroxylase (120) 120
heterozygote (120) 120
cyp21a2 (116) 116
cyp21 (115) 115
population (115) 115
prevalence (115) 115
dna mutational analysis (114) 114
adrenal hyperplasia, congenital - metabolism (113) 113
androgens (112) 112
fertility (111) 111
expression (110) 110
polycystic-ovary-syndrome (108) 108
research (108) 108
medicine & public health (106) 106
management (104) 104
testosterone (103) 103
steroids (99) 99
adrenocorticotropic hormone (98) 98
corticosteroids (98) 98
abridged index medicus (96) 96
ambiguous genitalia (96) 96
hirsutism (96) 96
identification (96) 96
neonatal screening (96) 96
cah (94) 94
major histocompatibility complex (94) 94
17-alpha-hydroxyprogesterone (93) 93
gene frequency (92) 92
hyperandrogenism (92) 92
gene deletion (91) 91
case-control studies (90) 90
cortisol (90) 90
growth (90) 90
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (2558) 2558
French (44) 44
Spanish (44) 44
German (42) 42
Chinese (21) 21
Portuguese (19) 19
Japanese (11) 11
Polish (11) 11
Russian (7) 7
Czech (4) 4
Italian (4) 4
Korean (4) 4
Croatian (3) 3
Dutch (3) 3
Hungarian (3) 3
Turkish (3) 3
Serbian (2) 2
Hebrew (1) 1
Swedish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Journal Article
Journal Article
Journal Article
Trends in Endocrinology & Metabolism, ISSN 1043-2760, 2008, Volume 19, Issue 3, pp. 96 - 99
Congenital adrenal hyperplasia due to steroid 11β-hydroxylase deficiency is a genetic disorder of steroidogenesis, transmitted as an autosomal recessive trait.... 
Endocrinology & Metabolism | 21-HYDROXYLASE DEFICIENCY | ALDOSTERONE SYNTHASE | ENDOCRINOLOGY & METABOLISM | UNEQUAL CROSSING-OVER | BETA-HYDROXYLASE DEFICIENCY | 11-DEOXYCORTISOL | MUTATIONS | HYPERTENSION | AMNIOTIC-FLUID | PRENATAL-DIAGNOSIS | CYP11B1 GENE
Journal Article
Best Practice & Research: Clinical Endocrinology & Metabolism, ISSN 1521-690X, 2008, Volume 23, Issue 2, pp. 181 - 192
Journal Article