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Now showing items 1-5 of 5
A genomewide linkage scan for quantitative-trait loci for obesity phenotypes
Deng, HW; Deng, HY; Liu, YJ; Liu, YZ; Xu, FH; Shen, H.; Conway, T.; Li, JL; Huang, QY; Davies, KM; Recker, RR. A genomewide linkage scan for quantitative-trait loci for obesity phenotypes. American Journal of Human Genetics. 2002, MAY. 70(5):1138-1151.
Relevance of the genes for bone mass variation to susceptibility to osteoporotic fractures and its implications to gene search for complex human diseases
Deng, HW; Mahaney, MC; Willams, JT; Li, J.; Conway, T.; Davies, KM; Li, JL; Deng, HY; Recker, RR. Relevance of the genes for bone mass variation to susceptibility to osteoporotic fractures and its implications to gene search for complex human diseases. Genetic epidemiology. 2002, JAN. 22(1):12-25.
Evidence for a major gene for bone mineral density/content in human pedigrees identified via probands with extreme bone mineral density
Deng, HW; Livshits, G.; Yakovenko, K.; Xu, FH; Conway, T.; Davies, KM; Deng, H.; Recker, RR. Evidence for a major gene for bone mineral density/content in human pedigrees identified via probands with extreme bone mineral density. Annals of Human Genetics. 2002, JAN. 66:61-74.
A whole-genome linkage scan suggests several genomic regions potentially containing quantitative trait loci for osteoporosis
Deng, HW; Xu, FH; Huang, QY; Shen, H.; Deng, HY; Conway, T.; Liu, YJ; Liu, YZ; Li, JL; Zhang, HT; Davies, KM; Recker, RR. A whole-genome linkage scan suggests several genomic regions potentially containing quantitative trait loci for osteoporosis. Journal of Clinical Endocrinology & Metabolism. 2002, NOV. 87(11):5151-5159.
A whole-genome linkage scan suggests several genomic regions potentially containing QTLs underlying the variation of stature
Deng, HW; Xu, FH; Liu, YZ; Shen, H.; Deng, HY; Huang, QY; Liu, YJ; Conway, T.; Li, JL; Davies, KM; Recker, RR. A whole-genome linkage scan suggests several genomic regions potentially containing QTLs underlying the variation of stature. American Journal of Medical Genetics. 2002, NOV 15. 113(1):29-39.