Clinical and molecular characterization of Xia–Gibbs syndrome: expanding the phenotypic spectrum in a brazilian cohort (2025)
- Authors:
- Sennes, Maísa Ganz Sanchez
- Carvalho, Laura Machado Lara
- Castro, Matheus Augusto Araújo
- Toccoli, Giovana Manilli
- Farias, Sofia de Oliveira
- Fialho, Davi Mendes Campo
- Athayde, Larissa Sampaio de
- Melaragno, Maria Isabel
- Spolador, Gustavo Marquezani
- Otto, Paulo A
- Piai, Caroline Brandão
- Kok, Fernando
- Rosenberg, Carla
- Bertola, Débora Romeo
- Kim, Chong Ae
- Krepischi, Ana Cristina Victorino
- Sennes, Maísa Ganz Sanchez
- USP affiliated authors: CARVALHO, LAURA MACHADO LARA - IB ; OTTO, PAULO ALBERTO - IB ; KOK, FERNANDO - FM ; ROSENBERG, CARLA - IB ; BERTOLA, DÉBORA ROMEO - IB ; KIM, CHONG AE - FM ; KREPISCHI, ANA CRISTINA VICTORINO - IB ; TOCCOLI, GIOVANA MANILLI - ESALQ ; SENNES, MAÍSA GANZ SANCHEZ - IB ; CASTRO, MATHEUS AUGUSTO ARAÚJO - FM ; FARIAS, SOFIA DE OLIVEIRA - IB ; FIALHO, DAVI MENDES CAMPOS - IB ; SPOLADOR, GUSTAVO MARQUEZANI - FM
- Unidades: IB; FM; ESALQ
- DOI: 10.1111/cge.14777
- Subjects: DOENÇAS GENÉTICAS; FENÓTIPOS; MICROBIOLOGIA
- Agências de fomento:
- Language: Inglês
- Objetivos de Desenvolvimento Sustentável (ODS):
03. Saúde e bem-estar
- Imprenta:
- Publisher place: Hoboken, NJ
- Date published: 2025
- Source:
- Título: Clinical Genetics
- ISSN: 1399-0004
- Volume/Número/Paginação/Ano: v. 108, n. 6, p. 654-663, 2025
- Este artigo possui versão em acesso aberto
- URL de acesso aberto
- PDF de acesso aberto
- Versão do Documento: Versão publicada (Published version)
-
Status: Artigo aberto em periódico híbrido (Hybrid Open Access) -
ABNT
SENNES, Maísa Ganz Sanchez et al. Clinical and molecular characterization of Xia–Gibbs syndrome: expanding the phenotypic spectrum in a brazilian cohort. Clinical Genetics, v. 108, n. 6, p. 654-663, 2025Tradução . . Disponível em: https://doi.org/10.1111/cge.14777. Acesso em: 13 mar. 2026. -
APA
Sennes, M. G. S., Carvalho, L. M. L., Castro, M. A. A., Toccoli, G. M., Farias, S. de O., Fialho, D. M. C., et al. (2025). Clinical and molecular characterization of Xia–Gibbs syndrome: expanding the phenotypic spectrum in a brazilian cohort. Clinical Genetics, 108( 6), 654-663. doi:10.1111/cge.14777 -
NLM
Sennes MGS, Carvalho LML, Castro MAA, Toccoli GM, Farias S de O, Fialho DMC, Athayde LS de, Melaragno MI, Spolador GM, Otto PA, Piai CB, Kok F, Rosenberg C, Bertola DR, Kim CA, Krepischi ACV. Clinical and molecular characterization of Xia–Gibbs syndrome: expanding the phenotypic spectrum in a brazilian cohort [Internet]. Clinical Genetics. 2025 ; 108( 6): 654-663.[citado 2026 mar. 13 ] Available from: https://doi.org/10.1111/cge.14777 -
Vancouver
Sennes MGS, Carvalho LML, Castro MAA, Toccoli GM, Farias S de O, Fialho DMC, Athayde LS de, Melaragno MI, Spolador GM, Otto PA, Piai CB, Kok F, Rosenberg C, Bertola DR, Kim CA, Krepischi ACV. Clinical and molecular characterization of Xia–Gibbs syndrome: expanding the phenotypic spectrum in a brazilian cohort [Internet]. Clinical Genetics. 2025 ; 108( 6): 654-663.[citado 2026 mar. 13 ] Available from: https://doi.org/10.1111/cge.14777 - SCAF4-related syndromic intellectual disability
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