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Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
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Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Bachega, Tânia A. S. S. ; Billerbeck, Ana E. C. ; Marcondes, José A. M. ; Madureira, Guiomar ; Arnhold, Ivo J. P. ; Mendonca, Berenice B.

Clinical endocrinology (Oxford), 2000-05, Vol.52 (5), p.601-607 [Periódico revisado por pares]

Oxford BSL: Blackwell Science Ltd

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2
Detection of Leptospira DNA in Patients with Aseptic Meningitis by PCR
Detection of Leptospira DNA in Patients with Aseptic Meningitis by PCR
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Detection of Leptospira DNA in Patients with Aseptic Meningitis by PCR

ROMERO, E. C ; BILLERBECK, A. E. C ; LANDO, V. S ; CAMARGO, E. D ; SOUZA, C. C ; YASUDA, P. H

Journal of Clinical Microbiology, 1998-05, Vol.36 (5), p.1453-1455 [Periódico revisado por pares]

Washington, DC: American Society for Microbiology

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3
A novel missense mutation (S18N) in the 5' non-HMG box region of the SRY gene in a patient with partial gonadal dysgenesis and his normal male relatives
A novel missense mutation (S18N) in the 5' non-HMG box region of the SRY gene in a patient with partial gonadal dysgenesis and his normal male relatives
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A novel missense mutation (S18N) in the 5' non-HMG box region of the SRY gene in a patient with partial gonadal dysgenesis and his normal male relatives

DOMENICE, S ; NISHI, M. Y ; BILHARINHO MENDONCA, B ; CORREIA BILLERBECK, A. E ; LATRONICO, A. C ; MEDEIROS, M. A ; RUSSELL, A. J ; VASS, K ; CARVALHO, F. M ; COSTA FRADE, E. M ; PRADO ARNHOLD, I. J

Human genetics, 1998-02, Vol.102 (2), p.213-215 [Periódico revisado por pares]

Heidelberg: Springer

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4
A novel point mutation (R840S) in the androgen receptor in a Brazilian family with partial androgen insensitivity syndrome
A novel point mutation (R840S) in the androgen receptor in a Brazilian family with partial androgen insensitivity syndrome
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A novel point mutation (R840S) in the androgen receptor in a Brazilian family with partial androgen insensitivity syndrome

Melo, Karla F.S. ; Latronico, Ana Claudia ; Costa, Elaine M.F. ; Billerbeck, Ana Elisa C. ; Mendonca, Berenice B. ; Arnhold, Ivo J.P.

Human mutation, 1999-10, Vol.14 (4), p.353-353 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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5
Parentage Testing on Blood Crusts from Firearms Projectiles by DNA Typing Settles an Insurance Fraud Case
Parentage Testing on Blood Crusts from Firearms Projectiles by DNA Typing Settles an Insurance Fraud Case
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Parentage Testing on Blood Crusts from Firearms Projectiles by DNA Typing Settles an Insurance Fraud Case

Soares-Vieira, JA ; Billerbeck, AEC ; Iwamura, ESM ; Cardoso, LA ; Muñoz, DR

Journal of forensic sciences, 2000-09, Vol.45 (5), p.1142-1143 [Periódico revisado por pares]

United States

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6
Allele and Genotype Frequencies for D1S80 Locus in a Brazilian Population Sample
Allele and Genotype Frequencies for D1S80 Locus in a Brazilian Population Sample
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Allele and Genotype Frequencies for D1S80 Locus in a Brazilian Population Sample

Soares-Vieira, JA ; Billerbeck, AEC ; Iwamura, ESM ; Muñoz, DR ; Otto, PA

Journal of forensic sciences, 2000-05, Vol.45 (3), p.696-697 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

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7
Investigation of the ZFY gene in XX true hermaphroditism and Swyer syndrome
Investigation of the ZFY gene in XX true hermaphroditism and Swyer syndrome
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Investigation of the ZFY gene in XX true hermaphroditism and Swyer syndrome

Damiani, D ; Billerbeck, A E ; Goldberg, A C ; Setian, N ; Fellous, M ; Kalil, J

Human genetics, 1990-06, Vol.85 (1), p.85-88 [Periódico revisado por pares]

Germany

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8
Low frequency of CYP2B deletions in Brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylas deficiency
Low frequency of CYP2B deletions in Brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylas deficiency
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Low frequency of CYP2B deletions in Brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylas deficiency

Bachega, T A ; Billerbeck, A E ; Madureira, G ; Arnhold, I J ; Medeiros, M A ; Marcondes, J A ; Longui, C A ; Nicolau, W ; Bloise, W ; Mendonca, B B

Human heredity, 1999-01, Vol.49 (1), p.9-14 [Periódico revisado por pares]

Switzerland

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9
A Microdeletion in the Ligand Binding Domain of Human Steroidogenic Factor 1 Causes XY Sex Reversal without Adrenal Insufficiency
A Microdeletion in the Ligand Binding Domain of Human Steroidogenic Factor 1 Causes XY Sex Reversal without Adrenal Insufficiency
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A Microdeletion in the Ligand Binding Domain of Human Steroidogenic Factor 1 Causes XY Sex Reversal without Adrenal Insufficiency

Correa, Rafaela V ; Domenice, Sorahia ; Bingham, Nathan C ; Billerbeck, Ana Elisa C ; Rainey, William E ; Parker, Keith L ; Mendonca, Berenice B

The journal of clinical endocrinology and metabolism, 2004-04, Vol.89 (4), p.1767-1772 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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10
Clinical, Hormonal, Behavioral, and Genetic Characteristics of Androgen Insensitivity Syndrome in a Brazilian Cohort: Five Novel Mutations in the Androgen Receptor Gene
Clinical, Hormonal, Behavioral, and Genetic Characteristics of Androgen Insensitivity Syndrome in a Brazilian Cohort: Five Novel Mutations in the Androgen Receptor Gene
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Clinical, Hormonal, Behavioral, and Genetic Characteristics of Androgen Insensitivity Syndrome in a Brazilian Cohort: Five Novel Mutations in the Androgen Receptor Gene

Melo, Karla F. S ; Mendonca, Berenice B ; Billerbeck, Ana Elisa C ; Costa, Elaine M. F ; Inácio, Marlene ; Silva, Frederico A. Q ; Leal, Angela M. O ; Latronico, Ana C ; Arnhold, Ivo J. P

The journal of clinical endocrinology and metabolism, 2003-07, Vol.88 (7), p.3241-3250 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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