Clinical and cytogenetic impact of maternal balanced double translocation: a familial case of 15q11.2 microduplication and microdeletion syndromes with genetic counselling implications (2024)
- Authors:
- USP affiliated authors: ROSENBERG, CARLA - IB ; MAZZONETTO, PATRICIA CAMACHO - IB
- Unidade: IB
- DOI: 10.3390/genes15121546
- Subjects: ACONSELHAMENTO GENÉTICO; DOENÇAS GENÉTICAS; DELEÇÃO DE GENES
- Agências de fomento:
- Language: Inglês
- Objetivos de Desenvolvimento Sustentável (ODS):
03. Saúde e bem-estar
- Imprenta:
- Source:
- Status:
- Artigo publicado em periódico de acesso aberto (Gold Open Access)
- Versão do Documento:
- Versão publicada (Published version)
- Acessar versão aberta:
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ABNT
VIEIRA, Daniela Koeller R e ROSENBERG, Carla e MAZZONETTO, Patricia Camacho. Clinical and cytogenetic impact of maternal balanced double translocation: a familial case of 15q11.2 microduplication and microdeletion syndromes with genetic counselling implications. Genes, v. 15, n. 12, 2024Tradução . . Disponível em: https://doi.org/10.3390/genes15121546. Acesso em: 07 maio 2026. -
APA
Vieira, D. K. R., Rosenberg, C., & Mazzonetto, P. C. (2024). Clinical and cytogenetic impact of maternal balanced double translocation: a familial case of 15q11.2 microduplication and microdeletion syndromes with genetic counselling implications. Genes, 15( 12). doi:10.3390/genes15121546 -
NLM
Vieira DKR, Rosenberg C, Mazzonetto PC. Clinical and cytogenetic impact of maternal balanced double translocation: a familial case of 15q11.2 microduplication and microdeletion syndromes with genetic counselling implications [Internet]. Genes. 2024 ; 15( 12):[citado 2026 maio 07 ] Available from: https://doi.org/10.3390/genes15121546 -
Vancouver
Vieira DKR, Rosenberg C, Mazzonetto PC. Clinical and cytogenetic impact of maternal balanced double translocation: a familial case of 15q11.2 microduplication and microdeletion syndromes with genetic counselling implications [Internet]. Genes. 2024 ; 15( 12):[citado 2026 maio 07 ] Available from: https://doi.org/10.3390/genes15121546 - Array-CGH analysis in patients with Goldenhar Syndrome
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