Plastic bronchitis in Noonan syndrome: further evidence suggesting a higher risk of lymphatic abnormalities in individuals harboring variants in PTPN11 residue p.Phe285 (2025)
- Authors:
- Autor USP: KIM, CHONG AE - FM
- Unidade: FM
- DOI: 10.1159/000540570
- Subjects: PNEUMOPATIAS; BRONQUITE; FENÓTIPOS; GENÓTIPOS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Molecular Syndromology
- ISSN: 1661-8769
- Volume/Número/Paginação/Ano: v. 16, n. 2, p. 165-170, 2025
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
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ABNT
PIRES, Lucas Vieira Lacerda et al. Plastic bronchitis in Noonan syndrome: further evidence suggesting a higher risk of lymphatic abnormalities in individuals harboring variants in PTPN11 residue p.Phe285. Molecular Syndromology, v. 16, n. 2, p. 165-170, 2025Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/87259. Acesso em: 18 fev. 2026. -
APA
Pires, L. V. L., Cas, E. D., Melo, L. C. de, Nakaie, C. M. A., Aiello, V. D., Yamamoto, G. L., et al. (2025). Plastic bronchitis in Noonan syndrome: further evidence suggesting a higher risk of lymphatic abnormalities in individuals harboring variants in PTPN11 residue p.Phe285. Molecular Syndromology, 16( 2), 165-170. doi:10.1159/000540570 -
NLM
Pires LVL, Cas ED, Melo LC de, Nakaie CMA, Aiello VD, Yamamoto GL, Honjo RS, Kim CA, Bertola DR. Plastic bronchitis in Noonan syndrome: further evidence suggesting a higher risk of lymphatic abnormalities in individuals harboring variants in PTPN11 residue p.Phe285 [Internet]. Molecular Syndromology. 2025 ; 16( 2): 165-170.[citado 2026 fev. 18 ] Available from: https://observatorio.fm.usp.br/handle/OPI/87259 -
Vancouver
Pires LVL, Cas ED, Melo LC de, Nakaie CMA, Aiello VD, Yamamoto GL, Honjo RS, Kim CA, Bertola DR. Plastic bronchitis in Noonan syndrome: further evidence suggesting a higher risk of lymphatic abnormalities in individuals harboring variants in PTPN11 residue p.Phe285 [Internet]. Molecular Syndromology. 2025 ; 16( 2): 165-170.[citado 2026 fev. 18 ] Available from: https://observatorio.fm.usp.br/handle/OPI/87259 - 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: 10.1159/000540570 (Fonte: oaDOI API)
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