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(Reference retrieved automatically from Google Scholar through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Novel deletion alleles carrying CYP21A1P/A2 chimeric genes in Brazilian patients with 21-hydroxylase deficiency

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Coeli‚ F. ; Soardi‚ F. ; Bernardi‚ R. ; De Araújo‚ M. ; Paulino‚ L. ; Lau‚ I. ; Petroli‚ R. ; de Lemos-Marini‚ S. ; Baptista‚ M. ; Guerra-Júnior‚ G. ; others
Total Authors: 11
Document type: Journal article
Source: BMC MEDICAL GENETICS; v. 11, n. 1, p. 104, 2010.
FAPESP's process: 05/00981-5 - Congenital adrenal hyperplasia: new mutations and their effects on the enzymatic activity
Grantee:Maricilda Palandi de Mello
Support type: Regular Research Grants