Variants in candidate genes for phenotype heterogeneity in patients with the 22q11.2 deletion syndrome (2024)
- Authors:
- Autor USP: KIM, CHONG AE - FM
- Unidade: FM
- DOI: 10.1155/2024/5549592
- Subjects: DOENÇAS CARDIOVASCULARES; DOENÇAS GENÉTICAS; FENÓTIPOS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Genetics research
- ISSN: 0016-6723
- Volume/Número/Paginação/Ano: v. 2024, article ID 5549592, 9p, 2024
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
NUNES, Natalia et al. Variants in candidate genes for phenotype heterogeneity in patients with the 22q11.2 deletion syndrome. Genetics research, v. 2024, 2024Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/77009. Acesso em: 27 fev. 2026. -
APA
Nunes, N., Nunes, B. C., Zamariolli, M., Soares, D. C. de Q., Santos, L. C. dos, Dantas, A. G., et al. (2024). Variants in candidate genes for phenotype heterogeneity in patients with the 22q11.2 deletion syndrome. Genetics research, 2024. doi:10.1155/2024/5549592 -
NLM
Nunes N, Nunes BC, Zamariolli M, Soares DC de Q, Santos LC dos, Dantas AG, Meloni VA, Belangero SI, Gil-da-Silva-Lopes VL, Kim CA, Melaragno MI. Variants in candidate genes for phenotype heterogeneity in patients with the 22q11.2 deletion syndrome [Internet]. Genetics research. 2024 ; 2024[citado 2026 fev. 27 ] Available from: https://observatorio.fm.usp.br/handle/OPI/77009 -
Vancouver
Nunes N, Nunes BC, Zamariolli M, Soares DC de Q, Santos LC dos, Dantas AG, Meloni VA, Belangero SI, Gil-da-Silva-Lopes VL, Kim CA, Melaragno MI. Variants in candidate genes for phenotype heterogeneity in patients with the 22q11.2 deletion syndrome [Internet]. Genetics research. 2024 ; 2024[citado 2026 fev. 27 ] Available from: https://observatorio.fm.usp.br/handle/OPI/77009 - NK and B cell deficiency in a MPS type II family with novel mutation in the IDS gene
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Informações sobre o DOI: 10.1155/2024/5549592 (Fonte: oaDOI API)
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