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
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

Access to Document

10.1203/00006450-199702000-00037

Cite this

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

@article{970dd099e52f4f35ad79ef23de3d0119,

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",

volume = "41",

pages = "302",

journal = "Pediatric Research",

issn = "0031-3998",

publisher = "Lippincott Williams and Wilkins Ltd.",

number = "2",

}

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

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

Y1 - 1997/2

UR - http://www.scopus.com/inward/record.url?scp=85026161101&partnerID=8YFLogxK

U2 - 10.1203/00006450-199702000-00037

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 -