High-resolution mapping by YAC fragmentation of a 2.5-Mb Xp22 region containing the human RS, KFSD and CLS disease genes.

Van de Vosse, E; Van der Bent, P; Heus, J J; Van Ommen, G J; Den Dunnen, J T

Van de Vosse, E; Van der Bent, P; Heus, J J; Van Ommen, G J; Den Dunnen, J T.

Affiliation

Van de Vosse E; MGC-Department of Human Genetics, Leiden University, Wassenaarseweg 72, 2333 AL Leiden, The Netherlands.

Mamm Genome ; 8(7): 497-501, 1997 Jul.

Article in En | MEDLINE | ID: mdl-9195994

Subject(s)

Bone Diseases, Developmental/genetics; Chromosome Mapping/methods; Darier Disease/genetics; Retinal Degeneration/genetics; X Chromosome; Abnormalities, Multiple/genetics; Blotting, Southern; Chromosomes, Artificial, Yeast; Cloning, Molecular; Cosmids; DNA Fragmentation; Electrophoresis, Gel, Pulsed-Field; Genetic Markers; Humans; Intellectual Disability/genetics; Restriction Mapping; Syndrome

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Collection: 01-internacional Database: MEDLINE Main subject: Retinal Degeneration / X Chromosome / Bone Diseases, Developmental / Chromosome Mapping / Darier Disease Limits: Humans Language: En Journal: Mamm Genome Journal subject: GENETICA Year: 1997 Document type: Article Affiliation country: Netherlands

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