Your browser doesn't support javascript.
loading
Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studies.
Zink, A M; Wohlleber, E; Engels, H; Rødningen, O K; Ravn, K; Heilmann, S; Rehnitz, J; Katzorke, N; Kraus, C; Blichfeldt, S; Hoffmann, P; Reutter, H; Brockschmidt, F F; Kreiß-Nachtsheim, M; Vogt, P H; Prescott, T E; Tümer, Z; Lee, J A.
Afiliação
  • Zink AM; Institute of Human Genetics, Rheinische Friedrich-Wilhelms-University, Bonn, Germany.
  • Wohlleber E; Institute of Human Genetics, Rheinische Friedrich-Wilhelms-University, Bonn, Germany.
  • Engels H; Institute of Human Genetics, Rheinische Friedrich-Wilhelms-University, Bonn, Germany.
  • Rødningen OK; Department of Medical Genetics, Oslo University Hospital, Oslo, Norway.
  • Ravn K; Applied Human Molecular Genetics, Kennedy Center, Glostrup, Denmark.
  • Heilmann S; Institute of Human Genetics, Rheinische Friedrich-Wilhelms-University, Bonn, Germany ; Department of Genomics, Life & Brain Center, Rheinische Friedrich-Wilhelms-University, Bonn, Germany.
  • Rehnitz J; Molecular Genetics and Infertility Unit, Department of Gynecology, Endocrinology and Reproductive Medicine, University Women Hospital, Heidelberg, Germany.
  • Katzorke N; Molecular Genetics and Infertility Unit, Department of Gynecology, Endocrinology and Reproductive Medicine, University Women Hospital, Heidelberg, Germany.
  • Kraus C; Institute of Human Genetics, Friedrich-Alexander-University, Erlangen-Nuremberg, Germany.
  • Blichfeldt S; Pediatric Department L55, Glostrup University Hospital, Glostrup, Denmark.
  • Hoffmann P; Institute of Human Genetics, Rheinische Friedrich-Wilhelms-University, Bonn, Germany ; Department of Genomics, Life & Brain Center, Rheinische Friedrich-Wilhelms-University, Bonn, Germany ; Medical Genetics, Department of Biomedicine, University Hospital, Basel, Switzerland.
  • Reutter H; Institute of Human Genetics, Rheinische Friedrich-Wilhelms-University, Bonn, Germany ; Department of Neonatology, Children's Hospital, Rheinische Friedrich-Wilhelms-University, Bonn, Germany.
  • Brockschmidt FF; Institute of Human Genetics, Rheinische Friedrich-Wilhelms-University, Bonn, Germany ; Department of Genomics, Life & Brain Center, Rheinische Friedrich-Wilhelms-University, Bonn, Germany.
  • Kreiß-Nachtsheim M; Institute of Human Genetics, Rheinische Friedrich-Wilhelms-University, Bonn, Germany.
  • Vogt PH; Molecular Genetics and Infertility Unit, Department of Gynecology, Endocrinology and Reproductive Medicine, University Women Hospital, Heidelberg, Germany.
  • Prescott TE; Department of Medical Genetics, Oslo University Hospital, Oslo, Norway.
  • Tümer Z; Applied Human Molecular Genetics, Kennedy Center, Glostrup, Denmark ; Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Lee JA; Institute of Human Genetics, Rheinische Friedrich-Wilhelms-University, Bonn, Germany ; Department of Genomics, Life & Brain Center, Rheinische Friedrich-Wilhelms-University, Bonn, Germany ; Greenwood Genetic Center, Greenwood, S.C., USA.
Mol Syndromol ; 5(2): 65-75, 2014 Feb.
Article em En | MEDLINE | ID: mdl-24715853
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Mol Syndromol Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Alemanha
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Mol Syndromol Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Alemanha