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Chinese Journal of Medical Genetics ; (6): 53-55, 2003.
Article Dans Chinois | WPRIM | ID: wpr-248501

Résumé

<p><b>OBJECTIVE</b>To evaluate the role of homozygosity mapping in the fine mapping of the genes responsible for the rare autosomal recessive diseases.</p><p><b>METHODS</b>Polymerase chain reaction-single sequence length polymorphism was used to genotype the family members from 8 families with osteoporosis-pseudoglioma syndrome(OPS) for 14 polymorphic loci within candidate region. The OPS candidate region was narrowed by searching for homozygous region in affected.</p><p><b>RESULTS</b>The OPS candidate region was narrowed to a 1 cM interval between D11S1296 and D11S4136.</p><p><b>CONCLUSION</b>Homozygosity mapping is a powerful method for mapping and narrowing the candidate region of the genes responsible for the rare autosomal recessive diseases.</p>


Sujets)
Femelle , Humains , Mâle , Malformations multiples , Génétique , Anatomopathologie , Cartographie chromosomique , Méthodes , Chromosomes humains de la paire 11 , Génétique , Maladies de l'oeil , Anatomopathologie , Santé de la famille , Prédisposition génétique à une maladie , Génétique , Homozygote , Répétitions microsatellites , Ostéogenèse imparfaite , Anatomopathologie , Pedigree , Syndrome
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