Your browser doesn't support javascript.
loading
Expanding the clinical spectrum of pathogenic variation in NR2F2: Asplenia.
Arsov, Todor; Kelecic, Jadranka; Frkovic, Sanda Huljev; Sestan, Mario; Kifer, Nastasia; Andrews, Dan; Adamski, Marcin; Jelusic, Marija; Cook, Matthew C.
Afiliação
  • Arsov T; Department of Immunology and Infectious Diseases, The John Curtin School of Medical Research, Australian National University, Canberra, Australia; Institute of Immunobiology and Human Genetics, Faculty of Medicine, University in Skopje, Skopje, Macedonia. Electronic address: todor.arsov@anu.edu.au.
  • Kelecic J; Department of Paediatrics, University of Zagreb School of Medicine, University Hospital Centre Zagreb, Zagreb, Croatia.
  • Frkovic SH; Department of Paediatrics, University of Zagreb School of Medicine, University Hospital Centre Zagreb, Zagreb, Croatia.
  • Sestan M; Department of Paediatrics, University of Zagreb School of Medicine, University Hospital Centre Zagreb, Zagreb, Croatia.
  • Kifer N; Department of Paediatrics, University of Zagreb School of Medicine, University Hospital Centre Zagreb, Zagreb, Croatia.
  • Andrews D; Department of Immunology and Infectious Diseases, The John Curtin School of Medical Research, Australian National University, Canberra, Australia.
  • Adamski M; Department of Immunology and Infectious Diseases, The John Curtin School of Medical Research, Australian National University, Canberra, Australia.
  • Jelusic M; Department of Paediatrics, University of Zagreb School of Medicine, University Hospital Centre Zagreb, Zagreb, Croatia.
  • Cook MC; Department of Immunology and Infectious Diseases, The John Curtin School of Medical Research, Australian National University, Canberra, Australia; Department of Immunology, The Canberra Hospital, Canberra, Australia.
Eur J Med Genet ; 64(12): 104347, 2021 Dec.
Article em En | MEDLINE | ID: mdl-34619368
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Fator II de Transcrição COUP / Síndrome de Heterotaxia Tipo de estudo: Prognostic_studies Limite: Child / Humans / Male Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Fator II de Transcrição COUP / Síndrome de Heterotaxia Tipo de estudo: Prognostic_studies Limite: Child / Humans / Male Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article