Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M I New

Showing results (231-240 of 292) with videos related to

Pageof 30
Sort By:
The Journal of Clinical Endocrinology and Metabolism|March 1, 1985
Late-onset adrenal steroid 3 beta-hydroxysteroid dehydrogenase deficiency. I. A cause of hirsutism in pubertal and postpubertal womenS Y Pang, A J Lerner, E Stoner, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1985
Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in manP C White, D Grossberger, B J Onufer, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1992
Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2L Pascoe, K M Curnow, L Slutsker, et al.
Lancet (London, England)|March 8, 1980
Autosomal dominant transmission and absence of HLA linkage in dexamethasone suppressible hyperaldosteronismM I New, S E Oberfield, L S Levine, et al.
Science (New York, N.Y.)|May 6, 1977
H-y antigen: expression in human subjects with the testicular feminization syndromeG C Koo, S S Wachtel, P Saenger, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1995
The R337C mutation generates a high Km 11 beta-hydroxysteroid dehydrogenase type II enzyme in a family with apparent mineralocorticoid excessV R Obeyesekere, P Ferrari, R K Andrews, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1974
Variation in pituitary-gonadal function in adolescent male homosexuals and heterosexualsG A Parks, S Korth-Schütz, R Penny, et al.
The Journal of Pediatrics|May 1, 1974
Juvenile hypertension caused by overproduction of renin within a renal segmentS P Bennett, L S Levine, E J Siegal, et al.
American Journal of Medical Genetics|October 23, 1997
Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) in CroatiaM Dumic, L Brkljacic, V Plavsic, et al.
Pediatric Research|December 14, 1999
Intrauterine growth retardation associated with maternal uniparental disomy for chromosome 6 unmasked by congenital adrenal hyperplasiaR P Spiro, S L Christian, D H Ledbetter, et al.
Pageof 30

Showing results (231-240 of 292) with videos related to

Sort By:
Pageof 30
The Journal of Clinical Endocrinology and Metabolism|March 1, 1985
Late-onset adrenal steroid 3 beta-hydroxysteroid dehydrogenase deficiency. I. A cause of hirsutism in pubertal and postpubertal womenS Y Pang, A J Lerner, E Stoner, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1985
Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in manP C White, D Grossberger, B J Onufer, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1992
Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2L Pascoe, K M Curnow, L Slutsker, et al.
Lancet (London, England)|March 8, 1980
Autosomal dominant transmission and absence of HLA linkage in dexamethasone suppressible hyperaldosteronismM I New, S E Oberfield, L S Levine, et al.
Science (New York, N.Y.)|May 6, 1977
H-y antigen: expression in human subjects with the testicular feminization syndromeG C Koo, S S Wachtel, P Saenger, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1995
The R337C mutation generates a high Km 11 beta-hydroxysteroid dehydrogenase type II enzyme in a family with apparent mineralocorticoid excessV R Obeyesekere, P Ferrari, R K Andrews, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1974
Variation in pituitary-gonadal function in adolescent male homosexuals and heterosexualsG A Parks, S Korth-Schütz, R Penny, et al.
The Journal of Pediatrics|May 1, 1974
Juvenile hypertension caused by overproduction of renin within a renal segmentS P Bennett, L S Levine, E J Siegal, et al.
American Journal of Medical Genetics|October 23, 1997
Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) in CroatiaM Dumic, L Brkljacic, V Plavsic, et al.
Pediatric Research|December 14, 1999
Intrauterine growth retardation associated with maternal uniparental disomy for chromosome 6 unmasked by congenital adrenal hyperplasiaR P Spiro, S L Christian, D H Ledbetter, et al.
Pageof 30