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The Journal of Clinical Endocrinology and Metabolism|August 18, 2000
Combined pituitary hormone deficiency caused by a novel mutation of a highly conserved residue (F88S) in the homeodomain of PROP-1M G Osorio, P Kopp, S Marui, et al.
The Journal of Clinical Endocrinology and Metabolism|February 18, 1999
17Beta-hydroxysteroid dehydrogenase 3 deficiency in womenB B Mendonca, I J Arnhold, W Bloise, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
Adrenocorticotropin-dependent precocious puberty of testicular origin in a boy with X-linked adrenal hypoplasia congenita due to a novel mutation in the DAX1 geneS Domenice, A C Latronico, V N Brito, et al.
Journal of Endocrinological Investigation|January 1, 1991
Identification of nonclassical 21-hydroxylase deficiency in girls with precocious pubarcheM V Leite, B B Mendonça, I J Arnhold, et al.
American Journal of Medical Genetics|September 1, 1984
Testicular regression in a patient with virilized female phenotypeC Rosenberg, Z Mustacchi, A Braz, et al.
Clinical Endocrinology|May 3, 2000
Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiencyT A Bachega, A E Billerbeck, J A Marcondes, et al.
The Journal of Clinical Endocrinology and Metabolism|March 20, 1999
Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 geneB B Mendonca, M G Osorio, A C Latronico, et al.
American Journal of Medical Genetics|August 1, 1994
Gonadal agenesis in XX and XY sisters: evidence for the involvement of an autosomal geneB B Mendonça, A S Barbosa, I J Arnhold, et al.
Human Mutation|January 1, 1995
Human androgen insensitivity due to point mutations encoding amino acid substitutions in the androgen receptor steroid-binding domainK Murono, B B Mendonca, I J Arnhold, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2001
Two novel mutations in the gonadotropin-releasing hormone receptor gene in Brazilian patients with hypogonadotropic hypogonadism and normal olfactionE M Costa, G Y Bedecarrats, B B Mendonca, et al.
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