Laboratorial diagnosis of the Fragile X syndrome: a fast, reliable and effective methodological approach supporting the Genetic Counseling services (2015)
- Authors:
- USP affiliated authors: MOLFETTA, GREICE ANDREOTTI DE - FMRP ; RAMOS, ESTER SILVEIRA - FMRP ; SILVA JUNIOR, WILSON ARAÚJO DA - FMRP
- Unidade: FMRP
- Subjects: SÍNDROME X; ACONSELHAMENTO GENÉTICO
- Language: Inglês
- Imprenta:
- Source:
- Título: Poster Abstracts
- Conference titles: Annual Meeting of the American Society of Human Genetics
-
ABNT
MOLFETTA, Greice Andreotti de et al. Laboratorial diagnosis of the Fragile X syndrome: a fast, reliable and effective methodological approach supporting the Genetic Counseling services. 2015, Anais.. Baltimore: ASHG, 2015. . Acesso em: 20 fev. 2026. -
APA
Molfetta, G. A. de, Marques, A., Furtado, C., Ramos, E. S., & Silva Júnior, W. A. da. (2015). Laboratorial diagnosis of the Fragile X syndrome: a fast, reliable and effective methodological approach supporting the Genetic Counseling services. In Poster Abstracts. Baltimore: ASHG. -
NLM
Molfetta GA de, Marques A, Furtado C, Ramos ES, Silva Júnior WA da. Laboratorial diagnosis of the Fragile X syndrome: a fast, reliable and effective methodological approach supporting the Genetic Counseling services. Poster Abstracts. 2015 ;[citado 2026 fev. 20 ] -
Vancouver
Molfetta GA de, Marques A, Furtado C, Ramos ES, Silva Júnior WA da. Laboratorial diagnosis of the Fragile X syndrome: a fast, reliable and effective methodological approach supporting the Genetic Counseling services. Poster Abstracts. 2015 ;[citado 2026 fev. 20 ] - Identification of a novel mutation Arg118Gly in the TWIST1 gene causing Saethre-Chotzen syndrome
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