Ontology highlight
ABSTRACT:
SUBMITTER: Rioux JD
PROVIDER: S-EPMC1377485 | biostudies-other | 1998 Oct
REPOSITORIES: biostudies-other
Rioux J D JD Stone V A VA Daly M J MJ Cargill M M Green T T Nguyen H H Nutman T T Zimmerman P A PA Tucker M A MA Hudson T T Goldstein A M AM Lander E E Lin A Y AY
American journal of human genetics 19981001 4
Familial eosinophilia (FE) is an autosomal dominant disorder characterized by peripheral hypereosinophilia of unidentifiable cause with or without other organ involvement. To localize the gene for FE, we performed a genomewide search in a large U.S. kindred, using 312 different polymorphic markers. Seventeen affected subjects, 28 unaffected bloodline relatives, and 8 spouses were genotyped. The initial linkage results from the genome scan provided evidence for linkage on chromosome 5q31-q33. Add ...[more]