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Fraser syndrome without cryptophthalmos: Two cases.
Boussion, S; Lyonnet, S; Van Der Zwaag, B; Vogel, M J; Smol, T; Mezel, A; Manouvrier-Hanu, S; Vincent-Delorme, C; Vanlerberghe, C.
Afiliação
  • Boussion S; CHU Lille, Clinique de Génétique, F-59000, Lille, France; Univ. Lille, RADEME, EA 7364, F-59000, Lille, France.
  • Lyonnet S; Service de Génétique Médicale et Institut Imagine, Inserm UMR1163, Hôpital universitaire Necker-Enfants malades, AP-HP, Paris, France.
  • Van Der Zwaag B; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Vogel MJ; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Smol T; Univ. Lille, RADEME, EA 7364, F-59000, Lille, France; CHU Lille, Institut de Génétique Médicale, F-59000, Lille, France.
  • Mezel A; CHU Lille, Service de chirurgie orthopédique pédiatrique, F-59000, Lille, France.
  • Manouvrier-Hanu S; CHU Lille, Clinique de Génétique, F-59000, Lille, France; Univ. Lille, RADEME, EA 7364, F-59000, Lille, France.
  • Vincent-Delorme C; CHU Lille, Clinique de Génétique, F-59000, Lille, France; Univ. Lille, RADEME, EA 7364, F-59000, Lille, France.
  • Vanlerberghe C; CHU Lille, Clinique de Génétique, F-59000, Lille, France; Univ. Lille, RADEME, EA 7364, F-59000, Lille, France. Electronic address: clemence.vanlerberghe@chru-lille.fr.
Eur J Med Genet ; 63(4): 103839, 2020 Apr.
Article em En | MEDLINE | ID: mdl-31923588
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas da Matriz Extracelular / Síndrome de Fraser Tipo de estudo: Prognostic_studies Limite: Child, preschool / Female / Humans / Infant Idioma: En Revista: Eur J Med Genet Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas da Matriz Extracelular / Síndrome de Fraser Tipo de estudo: Prognostic_studies Limite: Child, preschool / Female / Humans / Infant Idioma: En Revista: Eur J Med Genet Ano de publicação: 2020 Tipo de documento: Article