PDX1-MODY and dorsal pancreatic agenesis: New phenotype of a rare disease (2018)
- Authors:
- USP affiliated authors: ROCHA, MANOEL DE SOUZA - FM ; JORGE, ALEXANDER AUGUSTO DE LIMA - FM
- Unidade: FM
- DOI: 10.1111/cge.13044
- Subjects: DIABETES MELLITUS; TOMOGRAFIA COMPUTADORIZADA DE EMISSÃO; AGENESIA; PÂNCREAS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Clinical genetics
- ISSN: 0009-9163
- Volume/Número/Paginação/Ano: v. 93, n. 2, p. 382-386, 2018
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
CAETANO, L. A. e ROCHA, Manoel de Souza e JORGE, Alexander Augusto de Lima. PDX1-MODY and dorsal pancreatic agenesis: New phenotype of a rare disease. Clinical genetics, v. 93, n. 2, p. 382-386, 2018Tradução . . Disponível em: https://doi.org/10.1111/cge.13044. Acesso em: 24 fev. 2026. -
APA
Caetano, L. A., Rocha, M. de S., & Jorge, A. A. de L. (2018). PDX1-MODY and dorsal pancreatic agenesis: New phenotype of a rare disease. Clinical genetics, 93( 2), 382-386. doi:10.1111/cge.13044 -
NLM
Caetano LA, Rocha M de S, Jorge AA de L. PDX1-MODY and dorsal pancreatic agenesis: New phenotype of a rare disease [Internet]. Clinical genetics. 2018 ; 93( 2): 382-386.[citado 2026 fev. 24 ] Available from: https://doi.org/10.1111/cge.13044 -
Vancouver
Caetano LA, Rocha M de S, Jorge AA de L. PDX1-MODY and dorsal pancreatic agenesis: New phenotype of a rare disease [Internet]. Clinical genetics. 2018 ; 93( 2): 382-386.[citado 2026 fev. 24 ] Available from: https://doi.org/10.1111/cge.13044 - Use of a neutral gadolinium chelate as a contrast medium for ERCP: case report
- The E180splice mutation in the GHR gene causing Laron syndrome: Witness of a Sephardic Jewish exodus from the Iberian Peninsula to the New World?
- Clinical Characterization of Patients With Autosomal Dominant Short Stature due to Aggrecan Mutations
- Mutations in C-natriuretic peptide (NPPC): a novel cause of autosomal dominant short stature
- Aplicação da genética molecular no manejo dos distúrbios do crescimento
- Heterozygous Mutations in Natriuretic Peptide Receptor-B (NPR2) Gene as a Cause of Short Stature in Patients Initially Classified as Idiopathic Short Stature
- Development of a minimum dataset for the monitoring of recombinant human growth hormone (rhGH) therapy use in children with growth hormone deficiency (GHD) - a gloBE-reg initiative
- Clinical application of ACMG-AMP guidelines in HNF1A and GCK variants in a cohort of MODY families
- SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling
- Novel SUZ12 mutations in Weaver-like syndrome
Informações sobre o DOI: 10.1111/cge.13044 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas