Mechanism of pancreatic and liver malformations in human fetuses with short-rib polydactyly syndrome.

Loo, Christine K C; Pereira, Tamara N; Ramsing, Mette; Vogel, Ida; Petersen, Olav B; Ramm, Grant A

Loo, Christine K C; Pereira, Tamara N; Ramsing, Mette; Vogel, Ida; Petersen, Olav B; Ramm, Grant A.

Afiliação

Loo CK; Department of Anatomical Pathology SEALS, Prince of Wales Hospital, Sydney, Australia (formerly: Department of Anatomical Pathology, Royal Brisbane and Women's Hospital, Brisbane, Australia.).
Pereira TN; Hepatic Fibrosis Group, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Ramsing M; Discipline of Pathology School of Medicine, University of Western Sydney, Australia.
Vogel I; Hepatic Fibrosis Group, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Petersen OB; Department of Pathology, Aarhus University Hospital, Denmark.
Ramm GA; Department of Clinical Genetics, Aarhus University Hospital, Denmark.

Birth Defects Res A Clin Mol Teratol ; 106(7): 549-62, 2016 Jul.

Article em En | MEDLINE | ID: mdl-26970085

Assuntos

Feto; Fígado; Pâncreas; Síndrome de Costela Curta e Polidactilia; Feminino; Feto/anormalidades; Feto/embriologia; Humanos; Fígado/anormalidades; Fígado/embriologia; Masculino; Pâncreas/anormalidades; Pâncreas/embriologia; Síndrome de Costela Curta e Polidactilia/embriologia; Síndrome de Costela Curta e Polidactilia/patologia

Palavras-chave

ciliopathy; ductal plate malformation; human fetus; short-rib polydactyly

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pâncreas / Síndrome de Costela Curta e Polidactilia / Feto / Fígado Limite: Female / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article

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