Expanding the phenotype of 8p23.1 Deletion Syndrome: eight new cases resembling the clinical spectrum of 22q11.2 microdeletion (2023)
- Authors:
- Montenegro, Marilia Moreira
- Camilotti, Débora
- Quaio, Robledo D'angioli Costa
- Gasparini, Yanca
- Zanardo, Evelin Aline
- Rangel-Santos, Andreia
- Novo-Filho, Gil Monteiro
- Francisco, Gleyson
- Liro, Lucas
- Nascimento, Amom Mendes
- Chehimi, Samar Nasser
- Soares, Diogo Cordeiro Queiroz
- Krepischi, Ana Cristina Victorino
- Grassi, Marcília Sierro
- Honjo, Rachel Sayuri
- Palmeira, Patricia
- Kim, Chong Ae
- Carneiro-Sampaio, Magda Maria Sales
- Rosenberg, Carla
- Kulikowski, Leslie Domenici
- Montenegro, Marilia Moreira
- USP affiliated authors: KREPISCHI, ANA CRISTINA VICTORINO - IB ; JORGE, PATRICIA PALMEIRA DAENEKAS - FM ; KIM, CHONG AE - FM ; SAMPAIO, MAGDA MARIA SALES CARNEIRO - FM ; ROSENBERG, CARLA - IB ; KULIKOWSKI, LESLIE DOMENICI - FM ; MONTENEGRO, MARILIA MOREIRA - FM ; CAMILOTTI, DÉBORA - IB ; OLIVEIRA, YANCA GASPARINI DE - FM ; ZANARDO, EVELIN ALINE - FM ; NOVO FILHO, GIL MONTEIRO - FM ; CARVALHO, GLEYSON FRANCISCO DA SILVA - FM ; NASCIMENTO, AMOM MENDES - FM ; CHEHIMI, SAMAR NASSER - FM ; SOARES, DIOGO CORDEIRO DE QUEIROZ - FM ; GRASSI, MARCILIA SIERRO - FM ; KAWAHIRA, RACHEL SAYURI HONJO - FM
- Unidades: IB; FM
- DOI: 10.1016/j.jpeds.2022.08.051
- Subjects: GENÉTICA MÉDICA; DELEÇÃO DE GENES; ANORMALIDADES CONGÊNITAS; DOENÇAS RARAS
- Language: Inglês
- Imprenta:
- Publisher place: Philadelphia
- Date published: 2023
- Source:
- Título: The Journal of Pediatrics
- ISSN: 1097-6833
- Volume/Número/Paginação/Ano: v. 252, p. 56-60, Jan. 2023
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
MONTENEGRO, Marilia Moreira et al. Expanding the phenotype of 8p23.1 Deletion Syndrome: eight new cases resembling the clinical spectrum of 22q11.2 microdeletion. The Journal of Pediatrics, v. 252, n. Ja 2023, p. 56-60, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.jpeds.2022.08.051. Acesso em: 03 jan. 2026. -
APA
Montenegro, M. M., Camilotti, D., Quaio, R. D. 'angioli C., Gasparini, Y., Zanardo, E. A., Rangel-Santos, A., et al. (2023). Expanding the phenotype of 8p23.1 Deletion Syndrome: eight new cases resembling the clinical spectrum of 22q11.2 microdeletion. The Journal of Pediatrics, 252( Ja 2023), 56-60. doi:10.1016/j.jpeds.2022.08.051 -
NLM
Montenegro MM, Camilotti D, Quaio RD'angioli C, Gasparini Y, Zanardo EA, Rangel-Santos A, Novo-Filho GM, Francisco G, Liro L, Nascimento AM, Chehimi SN, Soares DCQ, Krepischi ACV, Grassi MS, Honjo RS, Palmeira P, Kim CA, Carneiro-Sampaio MMS, Rosenberg C, Kulikowski LD. Expanding the phenotype of 8p23.1 Deletion Syndrome: eight new cases resembling the clinical spectrum of 22q11.2 microdeletion [Internet]. The Journal of Pediatrics. 2023 ; 252( Ja 2023): 56-60.[citado 2026 jan. 03 ] Available from: https://doi.org/10.1016/j.jpeds.2022.08.051 -
Vancouver
Montenegro MM, Camilotti D, Quaio RD'angioli C, Gasparini Y, Zanardo EA, Rangel-Santos A, Novo-Filho GM, Francisco G, Liro L, Nascimento AM, Chehimi SN, Soares DCQ, Krepischi ACV, Grassi MS, Honjo RS, Palmeira P, Kim CA, Carneiro-Sampaio MMS, Rosenberg C, Kulikowski LD. Expanding the phenotype of 8p23.1 Deletion Syndrome: eight new cases resembling the clinical spectrum of 22q11.2 microdeletion [Internet]. The Journal of Pediatrics. 2023 ; 252( Ja 2023): 56-60.[citado 2026 jan. 03 ] Available from: https://doi.org/10.1016/j.jpeds.2022.08.051 - Lymphoproliferative disorder with polyautoimmunity and hypogammaglobulinemia: An unusual presentation of 22q11.2 deletion syndrome
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Informações sobre o DOI: 10.1016/j.jpeds.2022.08.051 (Fonte: oaDOI API)
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