Characterization of SCML1, a new gene in Xp22, with homology to developmental polycomb genes.

van de Vosse, E; Walpole, S M; Nicolaou, A; van der Bent, P; Cahn, A; Vaudin, M; Ross, M T; Durham, J; Pavitt, R; Wilkinson, J; Grafham, D; Bergen, A A; van Ommen, G J; Yates, J R; den Dunnen, J T; Trump, D

van de Vosse, E; Walpole, S M; Nicolaou, A; van der Bent, P; Cahn, A; Vaudin, M; Ross, M T; Durham, J; Pavitt, R; Wilkinson, J; Grafham, D; Bergen, A A; van Ommen, G J; Yates, J R; den Dunnen, J T; Trump, D.

Affiliation

van de Vosse E; MGC-Department of Human Genetics, Leiden University, Al Leiden, The Netherlands.

Genomics ; 49(1): 96-102, 1998 Apr 01.

Article in En | MEDLINE | ID: mdl-9570953

Subject(s)

Repressor Proteins/genetics; X Chromosome; Amino Acid Sequence; Animals; Base Sequence; DNA, Complementary; Eye Diseases, Hereditary/genetics; Humans; Molecular Sequence Data; Polycomb-Group Proteins; Retinal Degeneration/genetics

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Collection: 01-internacional Database: MEDLINE Main subject: Repressor Proteins / X Chromosome Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Genomics Journal subject: GENETICA Year: 1998 Document type: Article Affiliation country: Netherlands

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