Information and Diagnosis Networks – tools to improve diagnosis and treatment for patients with rare genetic diseases

Author:

Vieira Taiane Alves1ORCID,Trapp Franciele Barbosa2,Souza Carolina Fischinger Moura de2,Faccini Lavínia Schuler3ORCID,Jardim Laura Bannach3ORCID,Schwartz Ida Vanessa Doederlein3,Riegel Mariluce2ORCID,Vargas Carmen Regla2,Burin Maira Graeff2,Leistner-Segal Sandra2ORCID,Ashton-Prolla Patrícia4ORCID,Giugliani Roberto3ORCID

Affiliation:

1. Medical Genetics Service, Brazil; Research and Postgraduate Group, Brazil

2. Medical Genetics Service, Brazil

3. Medical Genetics Service, Brazil; Universidade Federal do Rio Grande do Sul, Brazil

4. Medical Genetics Service, Brazil; Research and Postgraduate Group, Brazil; Universidade Federal do Rio Grande do Sul, Brazil

Publisher

FapUNIFESP (SciELO)

Subject

Genetics,Molecular Biology

Reference37 articles.

1. The Brazilian Hereditary Cancer Network: Historical aspects and challenges for clinical cancer genetics in the public health care system in Brazil;Ashton-Prolla P;Genet Mol Biol,2016

2. Haplotype study in SCA10 families provides further evidence for a common ancestral origin of the mutation;Bampi GB;Neuromol Med,2017

3. Rede nacional de câncer familial: manual operacional,2009

4. Portaria 199, de 31 de janeiro de 2014,2014

5. Assessment of a pioneer metabolic information service in Brazil;Brustolin S;Community Genet,2006

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