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Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome.
Beysen, D; Raes, J; Leroy, B P; Lucassen, A; Yates, J R W; Clayton-Smith, J; Ilyina, H; Brooks, S Sklower; Christin-Maitre, S; Fellous, M; Fryns, J P; Kim, J R; Lapunzina, P; Lemyre, E; Meire, F; Messiaen, L M; Oley, C; Splitt, M; Thomson, J; Van de Peer, Y; Veitia, R A; De Paepe, A; De Baere, E.
Affiliation
  • Beysen D; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
Am J Hum Genet ; 77(2): 205-18, 2005 Aug.
Article in En | MEDLINE | ID: mdl-15962237
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / Blepharophimosis / DNA-Binding Proteins Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Animals / Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 2005 Document type: Article Affiliation country: Belgium Country of publication: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / Blepharophimosis / DNA-Binding Proteins Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Animals / Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 2005 Document type: Article Affiliation country: Belgium Country of publication: United States