An Xp22.1-p22.2 YAC contig encompassing the disease loci for RS, KFSD, CLS, HYP and RP15: Refined localization of RS

European Journal of Human Genetics

Volumn 4, Issue 2, 1996, Pages 101-104

  Van De Vosse, Esther ^a  

^a LEIDEN UNIVERSITY   (Netherlands)

Author keywords

Contig; Retinoschisis; Xp22

Indexed keywords

ARTICLE; CHROMOSOME XP; CONTROLLED STUDY; DARIER DISEASE; FEMALE; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENETIC RECOMBINATION; HUMAN; MALE; MARKER GENE; PRIORITY JOURNAL; RETINA DEGENERATION; RETINOSCHISIS; VITAMIN D RESISTANT RICKETS; YEAST ARTIFICIAL CHROMOSOME;

EID: 0029918833     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1159/000472177     Document Type: Article

References (1)

1. Bergen AAB, Ten Brink JB, Bleeker-Wagemakers LM, Van Schooneveld MJ: Refinement of the chromosomal position of the X-linked juvenile retinoschisis disease gene. J Med Genet 1994;31:972-975.