换一批
换一批Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions.
作者：
主题词
等位基因(Alleles);孤独性障碍(Autistic Disorder);儿童(Child);共病现象(Comorbidity);女(雌)性(Female);胃肠疾病(Gastrointestinal Diseases);疾病遗传易感性(Genetic Predisposition to Disease);基因型(Genotype);人类(Humans);连锁不平衡(Linkage Disequilibrium);男(雄)性(Male);表型(Phenotype);启动区, 遗传(Promoter Regions, Genetic);原癌基因蛋白质类(Proto-Oncogene Proteins);原癌基因蛋白质c-met(Proto-Oncogene Proteins c-met);受体, 生长因子(Receptors, Growth Factor);危险因素(Risk Factors);信号传导(Signal Transduction)
DOI
10.1542/peds.2008-0819
PMID
19255034
发布时间
2012-06-04
- 浏览22
Pediatrics
1018-24页
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