A comprehensive review of syndromic forms of obesity: genetic etiology, clinical features and molecular diagnosis (2024)
- Authors:
- USP affiliated authors: JORGE, ALEXANDER AUGUSTO DE LIMA - FM ; BERTOLA, DÉBORA ROMEO - IB ; KREPISCHI, ANA CRISTINA VICTORINO - IB ; ROSENBERG, CARLA - IB ; CARVALHO, LAURA MACHADO LARA - IB
- Unidades: FM; IB
- DOI: 10.1007/s13679-023-00543-y
- Subjects: OBESIDADE; GENÉTICA
- Keywords: Polifagia; Hiperfagia
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher place: Philadelphia, PA
- Date published: 2024
- Source:
- Título: Current Obesity Reports
- ISSN: 2162-4968
- Volume/Número/Paginação/Ano: 26 Jan. 2024
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
CARVALHO, Laura Machado Lara et al. A comprehensive review of syndromic forms of obesity: genetic etiology, clinical features and molecular diagnosis. Current Obesity Reports, n. 26 Ja 2024, 2024Tradução . . Disponível em: https://doi.org/10.1007/s13679-023-00543-y. Acesso em: 28 dez. 2025. -
APA
Carvalho, L. M. L., Jorge, A. A. de L., Bertola, D. R., Krepischi, A. C. V., & Rosenberg, C. (2024). A comprehensive review of syndromic forms of obesity: genetic etiology, clinical features and molecular diagnosis. Current Obesity Reports, (26 Ja 2024). doi:10.1007/s13679-023-00543-y -
NLM
Carvalho LML, Jorge AA de L, Bertola DR, Krepischi ACV, Rosenberg C. A comprehensive review of syndromic forms of obesity: genetic etiology, clinical features and molecular diagnosis [Internet]. Current Obesity Reports. 2024 ;(26 Ja 2024):[citado 2025 dez. 28 ] Available from: https://doi.org/10.1007/s13679-023-00543-y -
Vancouver
Carvalho LML, Jorge AA de L, Bertola DR, Krepischi ACV, Rosenberg C. A comprehensive review of syndromic forms of obesity: genetic etiology, clinical features and molecular diagnosis [Internet]. Current Obesity Reports. 2024 ;(26 Ja 2024):[citado 2025 dez. 28 ] Available from: https://doi.org/10.1007/s13679-023-00543-y - ACTB loss-of-function variant and AUTS2 duplication in a patient with syndromic intellectual disability
- EHMT2 as a Candidate Gene for an Autosomal Recessive Neurodevelopmental Syndrome
- Two novel pathogenic variants in MED13L: one familial and one isolated case
- A novel MYT1L mutation in a boy with syndromic obesity: case report and literature review
- SCAF4-related syndromic intellectual disability
- Cytogenetically visible inversions are formed by multiple molecular mechanisms
- LINE-1 hypermethylation in peripheral blood of cutaneous melanoma patients is associated with metastasis
- Rare germline copy number variations in hereditary cutaneous melanoma
- Lymphovascular invasion and histologic grade are associated with specific genomic profiles in invasive carcinomas of the breast
- Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways
Informações sobre o DOI: 10.1007/s13679-023-00543-y (Fonte: oaDOI API)
Download do texto completo
| Tipo | Nome | Link | |
|---|---|---|---|
 |
3180783.pdf | Direct link |
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
