标题
[NO TITLE AVAILABLE]
作者
关键词
-
出版物
GENETICS AND MOLECULAR BIOLOGY
Volume 37, Issue 1 suppl 1, Pages 263-270
出版商
FapUNIFESP (SciELO)
发表日期
2014-05-25
DOI
10.1590/s1415-47572014000200012
参考文献
相关参考文献
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- (2013) Raphael Machado de Castilhos et al. CEREBELLUM
- The Cuban program for predictive testing of SCA2: 11 years and 768 individuals to learn from
- (2013) T Cruz-Mariño et al. CLINICAL GENETICS
- What Counts as Effective Genetic Counselling for Presymptomatic Testing in Late-Onset Disorders? A Study of the Consultand’s Perspective
- (2013) Lídia Guimarães et al. Journal of Genetic Counseling
- Hereditary Ataxia and Spastic Paraplegia in Portugal
- (2013) Paula Coutinho et al. JAMA Neurology
- Recommendations for the predictive genetic test in Huntington's disease
- (2012) R MacLeod et al. CLINICAL GENETICS
- The Challenges of Incorporating Genetic Testing in the Unified National Health System in Brazil
- (2012) Débora Gusmão Melo et al. Genetic Testing and Molecular Biomarkers
- Psychological Well-Being and Family Satisfaction Levels Five Years After Being Confirmed as a Carrier of the Machado-Joseph Disease Mutation
- (2012) Carlos Gonzalez et al. Genetic Testing and Molecular Biomarkers
- Presymptomatic Testing for Neurogenetic Diseases in Brazil: Assessing Who Seeks and Who Follows through with Testing
- (2011) Caroline Santa Maria Rodrigues et al. Journal of Genetic Counseling
- Toward understanding Machado–Joseph disease
- (2011) Maria do Carmo Costa et al. PROGRESS IN NEUROBIOLOGY
- EMQN Best Practice Guidelines for molecular genetic testing of SCAs
- (2010) Jorge Sequeiros et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Role of the Disease in the Psychological Impact of Pre-Symptomatic Testing for SCA2 and FAP ATTRV30M: Experience with the Disease, Kinship and Gender of the Transmitting Parent
- (2009) Milena Paneque et al. Journal of Genetic Counseling
- Experience and outcome of 3 years of a European EQA scheme for genetic testing of the spinocerebellar ataxias
- (2008) Sara Seneca et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Decreasing uptake of predictive testing for Huntington's disease in a German centre: 12 years' experience (1993–2004)
- (2008) Christiane Bernhardt et al. EUROPEAN JOURNAL OF HUMAN GENETICS
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