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Showing results (181-190 of 292) with videos related to

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Clinical Endocrinology|April 1, 1984
Recovery of adrenal function after treatment of adrenocortical carcinoma with o,p'-DDDF Greig, S E Oberfield, L S Levine, et al.
American Journal of Human Genetics|September 1, 1988
Genetic mapping of the 21-hydroxylase locus: estimation of small recombination frequenciesC E Aston, S L Sherman, N E Morton, et al.
American Journal of Human Genetics|June 1, 1988
A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiencyS L Sherman, C E Aston, N E Morton, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1994
No evidence of mutations in the genes for type I and type II 3 beta-hydroxysteroid dehydrogenase (3 beta HSD) in nonclassical 3 beta HSD deficiencyM Zerah, E Rhéaume, P Mani, et al.
The Journal of Pediatrics|March 1, 1974
"True agonadism": a misnomer?G A Parks, K W Dumars, G A Limbeck, et al.
Human Genetics|December 1, 1992
Variants of the anti-Müllerian hormone gene in a compound heterozygote with the persistent Müllerian duct syndrome and his familyD Carré-Eusèbe, S Imbeaud, M Harbison, et al.
Molecular Endocrinology (Baltimore, Md.)|May 1, 1991
A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency alleleM T Tusie-Luna, P W Speiser, M Dumic, et al.
Developmental Pharmacology and Therapeutics|January 1, 1981
Ascorbic acid treatment in nephropathic cystinosis in identical twinsS E Oberfield, L S Levine, D Wellner, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1995
Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase geneR C Wilson, J Q Wei, K C Cheng, et al.
Acta Endocrinologica|April 1, 1983
The effects of long-term normalization of sodium balance on linear growth in disorders with aldosterone deficiencyU Kuhnle, A Rösler, J A Pareira, et al.
Pageof 30

Showing results (181-190 of 292) with videos related to

Sort By:
Pageof 30
Clinical Endocrinology|April 1, 1984
Recovery of adrenal function after treatment of adrenocortical carcinoma with o,p'-DDDF Greig, S E Oberfield, L S Levine, et al.
American Journal of Human Genetics|September 1, 1988
Genetic mapping of the 21-hydroxylase locus: estimation of small recombination frequenciesC E Aston, S L Sherman, N E Morton, et al.
American Journal of Human Genetics|June 1, 1988
A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiencyS L Sherman, C E Aston, N E Morton, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1994
No evidence of mutations in the genes for type I and type II 3 beta-hydroxysteroid dehydrogenase (3 beta HSD) in nonclassical 3 beta HSD deficiencyM Zerah, E Rhéaume, P Mani, et al.
The Journal of Pediatrics|March 1, 1974
"True agonadism": a misnomer?G A Parks, K W Dumars, G A Limbeck, et al.
Human Genetics|December 1, 1992
Variants of the anti-Müllerian hormone gene in a compound heterozygote with the persistent Müllerian duct syndrome and his familyD Carré-Eusèbe, S Imbeaud, M Harbison, et al.
Molecular Endocrinology (Baltimore, Md.)|May 1, 1991
A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency alleleM T Tusie-Luna, P W Speiser, M Dumic, et al.
Developmental Pharmacology and Therapeutics|January 1, 1981
Ascorbic acid treatment in nephropathic cystinosis in identical twinsS E Oberfield, L S Levine, D Wellner, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1995
Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase geneR C Wilson, J Q Wei, K C Cheng, et al.
Acta Endocrinologica|April 1, 1983
The effects of long-term normalization of sodium balance on linear growth in disorders with aldosterone deficiencyU Kuhnle, A Rösler, J A Pareira, et al.
Pageof 30