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Modeling age-specific facial development in Williams-Beuren-, Noonan-, and 22q11.2 deletion syndromes in cohorts of Czech patients aged 3-18 years: A cross-sectional three-dimensional geometric morphometry analysis of their facial gestalt.
Caplovicová, Martina; Moslerová, Veronika; Dupej, Ján; Macek, Milan; Zemková, Dana; Hoffmannová, Eva; Havlovicová, Markéta; Velemínská, Jana.
Afiliação
  • Caplovicová M; Department of Anthropology and Human Genetics, Faculty of Science, Charles University, Prague 2, Czech Republic.
  • Moslerová V; Department of Anthropology and Human Genetics, Faculty of Science, Charles University, Prague 2, Czech Republic.
  • Dupej J; Department of Biology and Medical Genetics, 2nd Faculty of Medicine, Charles University and Motol University Hospital, Prague 5, Czech Republic.
  • Macek M; Department of Anthropology and Human Genetics, Faculty of Science, Charles University, Prague 2, Czech Republic.
  • Zemková D; Department of Software and Computer Science, Faculty of Mathematics and Physics, Charles University, Prague 2, Czech Republic.
  • Hoffmannová E; Department of Biology and Medical Genetics, 2nd Faculty of Medicine, Charles University and Motol University Hospital, Prague 5, Czech Republic.
  • Havlovicová M; Department of Biology and Medical Genetics, 2nd Faculty of Medicine, Charles University and Motol University Hospital, Prague 5, Czech Republic.
  • Velemínská J; Department of Anthropology and Human Genetics, Faculty of Science, Charles University, Prague 2, Czech Republic.
Am J Med Genet A ; 176(12): 2604-2613, 2018 12.
Article em En | MEDLINE | ID: mdl-30380201
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Williams / Fácies / Imageamento Tridimensional / Síndrome de DiGeorge / Modelos Anatômicos / Síndrome de Noonan Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Male País como assunto: Europa Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Williams / Fácies / Imageamento Tridimensional / Síndrome de DiGeorge / Modelos Anatômicos / Síndrome de Noonan Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Male País como assunto: Europa Idioma: En Ano de publicação: 2018 Tipo de documento: Article