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Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis.
Bagheri, Hani; Badduke, Chansonette; Qiao, Ying; Colnaghi, Rita; Abramowicz, Iga; Alcantara, Diana; Dunham, Christopher; Wen, Jiadi; Wildin, Robert S; Nowaczyk, Malgorzata Jm; Eichmeyer, Jennifer; Lehman, Anna; Maranda, Bruno; Martell, Sally; Shan, Xianghong; Lewis, Suzanne Me; O'Driscoll, Mark; Gregory-Evans, Cheryl Y; Rajcan-Separovic, Evica.
Afiliação
  • Bagheri H; Department of Pathology and Laboratory Medicine, University of British Columbia (UBC), Vancouver, British Columbia, Canada.
  • Badduke C; Child and Family Research Institute, Vancouver, British Columbia, Canada.
  • Qiao Y; Department of Pathology and Laboratory Medicine, University of British Columbia (UBC), Vancouver, British Columbia, Canada.
  • Colnaghi R; Child and Family Research Institute, Vancouver, British Columbia, Canada.
  • Abramowicz I; Department of Pathology and Laboratory Medicine, University of British Columbia (UBC), Vancouver, British Columbia, Canada.
  • Alcantara D; Child and Family Research Institute, Vancouver, British Columbia, Canada.
  • Dunham C; Human DNA Damage Response Disorders Group, Genome Damage and Stability Centre, University of Sussex, Brighton, United Kingdom.
  • Wen J; Human DNA Damage Response Disorders Group, Genome Damage and Stability Centre, University of Sussex, Brighton, United Kingdom.
  • Wildin RS; Human DNA Damage Response Disorders Group, Genome Damage and Stability Centre, University of Sussex, Brighton, United Kingdom.
  • Nowaczyk MJ; Department of Pathology and Laboratory Medicine, University of British Columbia (UBC), Vancouver, British Columbia, Canada.
  • Eichmeyer J; University of Texas at Dallas, Dallas, Texas, USA.
  • Lehman A; St. Luke's Children's Hospital, Boise, Idaho, USA.
  • Maranda B; Department of Pathology and Molecular Medicine, McMaster University Medical Centre, Hamilton, Ontario, Canada.
  • Martell S; St. Luke's Mountain States Tumor Institute, Boise, Idaho, USA.
  • Shan X; Department of Medical Genetics, UBC, Vancouver, British Columbia, Canada.
  • Lewis SM; Medical Genetics, Université de Sherbrooke, Sherbrooke, Québec, Canada.
  • O'Driscoll M; Department of Pathology and Laboratory Medicine, University of British Columbia (UBC), Vancouver, British Columbia, Canada.
  • Gregory-Evans CY; Child and Family Research Institute, Vancouver, British Columbia, Canada.
  • Rajcan-Separovic E; Department of Ophthalmology, UBC, Vancouver, British Columbia, Canada.
JCI Insight ; 1(3): e85461, 2016 03 17.
Article em En | MEDLINE | ID: mdl-27699255
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Cromossomos Humanos Par 2 / Deleção Cromossômica / Transtornos Cromossômicos Tipo de estudo: Prognostic_studies Limite: Adolescent / Animals / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: JCI Insight Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Canadá País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Cromossomos Humanos Par 2 / Deleção Cromossômica / Transtornos Cromossômicos Tipo de estudo: Prognostic_studies Limite: Adolescent / Animals / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: JCI Insight Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Canadá País de publicação: Estados Unidos