Editorial: Early Genetic and Clinical Diagnosis in MEN1

Full text
Author(s):	Lourenco, Delmar M., Jr. ; de Herder, Wouter W. Total Authors: 2
Document type:	Journal article
Source:	FRONTIERS IN ENDOCRINOLOGY; v. 11, p. 4-pg., 2020-04-15.

FAPESP's process:	15/25444-4 - Visit of Prof. Dr. Stephen J. Marx at the University of São Paulo collaborating with translational research projects on hereditary endocrine neoplasia
Grantee:	Delmar Muniz Lourenço Jr
Support Opportunities:	Research Grants - Visiting Researcher Grant - International


FAPESP's process:	16/07504-2 - Clinical impact of the use of genetic panels based on next generation sequencing in the differential diagnosis of multiple endocrine neoplasia type 1 and analysis of potential genotype-phenotype correlations.
Grantee:	Delmar Muniz Lourenço Jr
Support Opportunities:	Regular Research Grants


FAPESP's process:	13/19810-2 - Evaluation of new generation sequencing efficiency in the analysis of MEN1, CDKN2B/p15, CDKN2C/p18 CDKN1A/p21, CDKN1B/p27Kip1 and AIP genes in patients with multiple endocrine neoplasia type 1 (MEN1)
Grantee:	Delmar Muniz Lourenço Jr
Support Opportunities:	Regular Research Grants