The power to detect genetic linkage for quantitative traits in the Utah CEPH pedigrees
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概要
- 論文の詳細を見る
- Springer-Verlag Tokyoの論文
- 2005-02-01
著者
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LEPPERT Mark
Department of Human Genetics
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Leppert Mark
Department Of Human Genetics Eccles Institute Of Human Genetics University Of Utah Health Sciences C
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MALHOTRA Alka
Department of Human Genetics, Eccles Institute of Human Genetics, University of Utah Health Sciences
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CROMER Kevin
Department of Human Genetics, Eccles Institute of Human Genetics, University of Utah Health Sciences
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HASSTEDT Sandra
Department of Human Genetics, Eccles Institute of Human Genetics, University of Utah Health Sciences
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Cromer Kevin
Department Of Human Genetics Eccles Institute Of Human Genetics University Of Utah Health Sciences C
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Malhotra Alka
Department Of Human Genetics Eccles Institute Of Human Genetics University Of Utah Health Sciences C
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Hasstedt Sandra
Department Of Human Genetics Eccles Institute Of Human Genetics University Of Utah Health Sciences C
関連論文
- Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcript
- The power to detect genetic linkage for quantitative traits in the Utah CEPH pedigrees
- Pleiotropy of type 2 diabetes with obesity
- Single nucleotide polymorphisms in JAZF1 and BCL11A gene are nominally associated with type 2 diabetes in African-American families from the GENNID study