Frequency of deletions and gene conversions in brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

T. A.S. Bachega; A. E.C. Billerbeck; G. Madureira; I. J.P. Amhold; M. I. New; W. Nicolau; J. A.M. Marcondes; C. A. Longui; M. A. Medeiros; W. Bloise; S. M.F. Villares; A. C. Bianco; B. B. Mendonça

doi:10.1203/00006450-199702000-00037

Frequency of deletions and gene conversions in brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

T. A.S. Bachega
, A. E.C. Billerbeck
, G. Madureira
, I. J.P. Amhold
, M. I. New
, W. Nicolau
, J. A.M. Marcondes
, C. A. Longui
, M. A. Medeiros
, W. Bloise
, S. M.F. Villares
, A. C. Bianco
, B. B. Mendonça

Research output: Contribution to journal › Article › peer-review

Original language	English (US)
Pages (from-to)	302
Number of pages	1
Journal	Pediatric Research
Volume	41
Issue number	2
DOIs	https://doi.org/10.1203/00006450-199702000-00037
State	Published - Feb 1997
Externally published	Yes

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health

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10.1203/00006450-199702000-00037

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Bachega, T. A. S., Billerbeck, A. E. C., Madureira, G., Amhold, I. J. P., New, M. I., Nicolau, W., Marcondes, J. A. M., Longui, C. A., Medeiros, M. A., Bloise, W., Villares, S. M. F., Bianco, A. C., & Mendonça, B. B. (1997). Frequency of deletions and gene conversions in brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Pediatric Research, 41(2), 302. https://doi.org/10.1203/00006450-199702000-00037

Bachega, TAS, Billerbeck, AEC, Madureira, G, Amhold, IJP, New, MI, Nicolau, W, Marcondes, JAM, Longui, CA, Medeiros, MA, Bloise, W, Villares, SMF, Bianco, AC & Mendonça, BB 1997, 'Frequency of deletions and gene conversions in brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency', Pediatric Research, vol. 41, no. 2, pp. 302. https://doi.org/10.1203/00006450-199702000-00037

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title = "Frequency of deletions and gene conversions in brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency",

author = "Bachega, \{T. A.S.\} and Billerbeck, \{A. E.C.\} and G. Madureira and Amhold, \{I. J.P.\} and New, \{M. I.\} and W. Nicolau and Marcondes, \{J. A.M.\} and Longui, \{C. A.\} and Medeiros, \{M. A.\} and W. Bloise and Villares, \{S. M.F.\} and Bianco, \{A. C.\} and Mendon{\c c}a, \{B. B.\}",

year = "1997",

month = feb,

doi = "10.1203/00006450-199702000-00037",

language = "English (US)",

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TY - JOUR

T1 - Frequency of deletions and gene conversions in brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

AU - Bachega, T. A.S.

AU - Billerbeck, A. E.C.

AU - Madureira, G.

AU - Amhold, I. J.P.

AU - New, M. I.

AU - Nicolau, W.

AU - Marcondes, J. A.M.

AU - Longui, C. A.

AU - Medeiros, M. A.

AU - Bloise, W.

AU - Villares, S. M.F.

AU - Bianco, A. C.

AU - Mendonça, B. B.

PY - 1997/2

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UR - https://www.scopus.com/pages/publications/85026161101#tab=citedBy

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DO - 10.1203/00006450-199702000-00037

M3 - Article

AN - SCOPUS:85026161101

SN - 0031-3998

VL - 41

SP - 302

JO - Pediatric Research

JF - Pediatric Research

IS - 2

ER -

Frequency of deletions and gene conversions in brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

ASJC Scopus subject areas

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