Your browser doesn't support javascript.
loading
The role of 22q11.2 deletion syndrome in the relationship between congenital heart disease and scoliosis.
Homans, Jelle F; de Reuver, Steven; Heung, Tracy; Silversides, Candice K; Oechslin, Erwin N; Houben, Michiel L; McDonald-McGinn, Donna M; Kruyt, Moyo C; Castelein, René M; Bassett, Anne S.
Afiliação
  • Homans JF; Department of Orthopedic Surgery, University Medical Center Utrecht, P.O. Box 85500, 3508 Utrecht, the Netherlands.
  • de Reuver S; Department of Orthopedic Surgery, University Medical Center Utrecht, P.O. Box 85500, 3508 Utrecht, the Netherlands.
  • Heung T; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, ON, Canada M5G 2N2; The Dalglish Family 22q Clinic for Adults, University Health Network, 200 Elizabeth St, Toronto, ON, Canada.
  • Silversides CK; The Dalglish Family 22q Clinic for Adults, University Health Network, 200 Elizabeth St, Toronto, ON, Canada; Toronto Congenital Cardiac Centre for Adults, Peter Munk Cardiac Centre, 585 University Ave, Toronto, ON, Canada M5G 2N2; Division of Cardiology, Department of Medicine, University Health Net
  • Oechslin EN; The Dalglish Family 22q Clinic for Adults, University Health Network, 200 Elizabeth St, Toronto, ON, Canada; Toronto Congenital Cardiac Centre for Adults, Peter Munk Cardiac Centre, 585 University Ave, Toronto, ON, Canada M5G 2N2; Division of Cardiology, Department of Medicine, University Health Net
  • Houben ML; Department of Pediatrics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • McDonald-McGinn DM; Division of Human Genetics, 22q and You Center, Children's Hospital of Philadelphia, Philadelphia, PA, USA; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Kruyt MC; Department of Orthopedic Surgery, University Medical Center Utrecht, P.O. Box 85500, 3508 Utrecht, the Netherlands.
  • Castelein RM; Department of Orthopedic Surgery, University Medical Center Utrecht, P.O. Box 85500, 3508 Utrecht, the Netherlands.
  • Bassett AS; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, ON, Canada M5G 2N2; The Dalglish Family 22q Clinic for Adults, University Health Network, 200 Elizabeth St, Toronto, ON, Canada; Toronto Congenital Cardiac Centre for Adults, Peter Munk Cardiac Centre, 585 Universit
Spine J ; 20(6): 956-963, 2020 06.
Article em En | MEDLINE | ID: mdl-31958577
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Escoliose / Síndrome de DiGeorge / Cardiopatias Congênitas / Síndrome de Marfan Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Child / Female / Humans País/Região como assunto: America do norte Idioma: En Revista: Spine J Assunto da revista: ORTOPEDIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Holanda
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Escoliose / Síndrome de DiGeorge / Cardiopatias Congênitas / Síndrome de Marfan Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Child / Female / Humans País/Região como assunto: America do norte Idioma: En Revista: Spine J Assunto da revista: ORTOPEDIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Holanda