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Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator.
Lumaka, A; Cosemans, N; Lulebo Mampasi, A; Mubungu, G; Mvuama, N; Lubala, T; Mbuyi-Musanzayi, S; Breckpot, J; Holvoet, M; de Ravel, T; Van Buggenhout, G; Peeters, H; Donnai, D; Mutesa, L; Verloes, A; Lukusa Tshilobo, P; Devriendt, K.
Afiliação
  • Lumaka A; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.
  • Cosemans N; Center for Human Genetics, Faculty of Medicine, University of Kinshasa, Kinshasa, DR Congo.
  • Lulebo Mampasi A; Department of Paediatrics, Faculty of Medicine, University of Kinshasa, Kinshasa, DR Congo.
  • Mubungu G; Institut National de Recherche Biomédicale, Kinshasa, DR Congo.
  • Mvuama N; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.
  • Lubala T; School of Public Health, Faculty of Medicine, University of Kinshasa, Kinshasa, DR Congo.
  • Mbuyi-Musanzayi S; Center for Human Genetics, Faculty of Medicine, University of Kinshasa, Kinshasa, DR Congo.
  • Breckpot J; Department of Paediatrics, Faculty of Medicine, University of Kinshasa, Kinshasa, DR Congo.
  • Holvoet M; School of Public Health, Faculty of Medicine, University of Kinshasa, Kinshasa, DR Congo.
  • de Ravel T; Sendwe University Hospitals, University of Lubumbashi, Lubumbashi, DR Congo.
  • Van Buggenhout G; Sendwe University Hospitals, University of Lubumbashi, Lubumbashi, DR Congo.
  • Peeters H; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.
  • Donnai D; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.
  • Mutesa L; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.
  • Verloes A; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.
  • Lukusa Tshilobo P; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.
  • Devriendt K; Manchester Centre for Genomic Medicine, Saint Mary's Hospital, Manchester Academic Health Science Centre, University of Manchester, Manchester, UK.
Clin Genet ; 92(2): 166-171, 2017 Aug.
Article em En | MEDLINE | ID: mdl-27925162
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Processamento de Imagem Assistida por Computador / Atrofia Muscular / Síndrome de Down / Anormalidades Craniofaciais / Deficiência Intelectual Tipo de estudo: Diagnostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Clin Genet Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Bélgica
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 / Processamento de Imagem Assistida por Computador / Atrofia Muscular / Síndrome de Down / Anormalidades Craniofaciais / Deficiência Intelectual Tipo de estudo: Diagnostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Clin Genet Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Bélgica