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article
human
Humans
6
controlled study
6
female
6
genotype
6
adult
5
gene mutation
5
Adrenal Hyperplasia, Congenital
4
Mutation
4
Steroid 21-Hydroxylase
4
allele
4
congenital adrenal hyperplasia
4
exon
4
heterozygosity
4
steroid 21 monooxygenase
4
Adolescent
3
Argentina
3
CYP21A2 protein, human
3
Case-Control Studies
3
Female
3
Premature ovarian failure
3
chemistry
3
follitropin
3
genetics
3
point mutation
3
premature ovarian failure
3
priority journal
3
steroid 21 monooxygenase deficiency
3
Adult
2
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1por Minutolo, C., Nadra, A.D., Fernández, C., Taboas, M., Buzzalino, N., Casali, B., Belli, S., Charreau, E.H., Alba, L., Dain, L.
Publicado 2011Artículo publishedVersion -
2Artículo publishedVersion
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6por Minutolo, C., Nadra, A.D., Fernández, C., Taboas, M., Buzzalino, N., Casali, B., Belli, S., Charreau, E.H., Alba, L., Dain, L.JOUR
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