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CHD7 deficiency in "Looper", a new mouse model of CHARGE syndrome, results in ossicle malformation, otosclerosis and hearing impairment.
Ogier, Jacqueline M; Carpinelli, Marina R; Arhatari, Benedicta D; Symons, R C Andrew; Kile, Benjamin T; Burt, Rachel A.
Afiliação
  • Ogier JM; Murdoch Childrens Research Institute, Parkville, Victoria, Australia.
  • Carpinelli MR; Murdoch Childrens Research Institute, Parkville, Victoria, Australia; The HEARing Cooperative Research Centre, Parkville, Victoria, Australia; Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia; Department of Medical Biology, University of Melbourne, Parkville, Victo
  • Arhatari BD; ARC Centre of Excellence for Coherent X-ray Science, Department of Physics, La Trobe University, Bundoora, Victoria, Australia.
  • Symons RC; Department of Ophthalmology, Royal Melbourne Hospital, Parkville, Victoria, Australia.
  • Kile BT; Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia; Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia; Department of Genetics, University of Melbourne, Parkville, Victoria, Australia.
  • Burt RA; Murdoch Childrens Research Institute, Parkville, Victoria, Australia; The HEARing Cooperative Research Centre, Parkville, Victoria, Australia; Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia; Department of Genetics, University of Melbourne, Parkville, Victoria, Au
PLoS One ; 9(5): e97559, 2014.
Article em En | MEDLINE | ID: mdl-24840056
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Otosclerose / Proteínas de Ligação a DNA / Síndrome CHARGE / Perda Auditiva Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Animals / Humans / Male Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Austrália
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Otosclerose / Proteínas de Ligação a DNA / Síndrome CHARGE / Perda Auditiva Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Animals / Humans / Male Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Austrália