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Article Dans Chinois | WPRIM | ID: wpr-287451

Résumé

<p><b>OBJECTIVE</b>To map the disease-causing gene in a Chinese family with autosomal dominant retinitis pigmentosa.</p><p><b>METHODS</b>Twenty-seven micro-satellite markers were randomly selected from the region around the known loci of causative genes, and haplotypes were determined by ABI3100 genetic analyzer. Two-point linkage analysis was performed using MLINK.</p><p><b>RESULTS</b>The Lod score of each marker vs adRP was below 1.</p><p><b>CONCLUSION</b>The phenotype of this family may not be caused by mutation of the known disease-causing genes.</p>


Sujets)
Femelle , Humains , Mâle , Asiatiques , Génétique , Chine , Gènes dominants , Liaison génétique , Dépistage génétique , Répétitions microsatellites , Génétique , Mutation , Pedigree , Phénotype , Rétinite pigmentaire , Diagnostic , Génétique , Anatomopathologie
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