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Application of homozygosity mapping to the fine mapping of the osteoporosis-pseudoglioma syndrome locus / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 53-55, 2003.
Article in Chinese | WPRIM | ID: wpr-248501
ABSTRACT
<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>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Osteogenesis Imperfecta / Pathology / Pedigree / Syndrome / Abnormalities, Multiple / Chromosomes, Human, Pair 11 / Family Health / Chromosome Mapping / Microsatellite Repeats / Genetic Predisposition to Disease Limits: Female / Humans / Male Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2003 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Osteogenesis Imperfecta / Pathology / Pedigree / Syndrome / Abnormalities, Multiple / Chromosomes, Human, Pair 11 / Family Health / Chromosome Mapping / Microsatellite Repeats / Genetic Predisposition to Disease Limits: Female / Humans / Male Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2003 Type: Article