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De novo 393 kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic features.
Varvagiannis, Konstantinos; Papoulidis, Ioannis; Koromila, Theodora; Kefalas, Konstantinos; Ziegler, Monika; Liehr, Thomas; Petersen, Michael B; Gyftodimou, Yolanda; Manolakos, Emmanouil.
Afiliação
  • Varvagiannis K; Department of Genetics, Institute of Child Health, Athens, Greece.
  • Papoulidis I; Eurogenetica S.A., Laboratory of Genetics, Athens-Thessaloniki, Greece.
  • Koromila T; Laboratory of Human Genetics, Department of Biology, University of Athens, Athens, Greece.
  • Kefalas K; Bioiatriki S.A., Laboratory of Genetics, Athens, Greece.
  • Ziegler M; Institute of Human Genetics Anthropology, Jena University Hospital, Jena, Germany.
  • Liehr T; Institute of Human Genetics Anthropology, Jena University Hospital, Jena, Germany.
  • Petersen MB; Department of Genetics, Institute of Child Health, Athens, Greece.
  • Gyftodimou Y; Department of Genetics, Institute of Child Health, Athens, Greece.
  • Manolakos E; Eurogenetica S.A., Laboratory of Genetics, Athens-Thessaloniki, Greece ; Cattedra di Genetica Medica, Ospedale Binaghi, Cagliari, Italy.
Meta Gene ; 2: 274-82, 2014 Dec.
Article em En | MEDLINE | ID: mdl-25606410
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Meta Gene Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Grécia
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Meta Gene Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Grécia