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Results: 1-7 |
Results: 7
Combined linkage and segregation analysis using regressive models
Authors: Ebow Bonney, George Lathrop, G. Mark Lalouel, Jean-Marc
Citation: Ebow Bonney, George et al., Combined linkage and segregation analysis using regressive models, American journal of human genetics , 43-I(1), 1988, pp. 29-37
Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5
Authors: Nakamura, Yusuke Lathrop, Mark Leppert, Mark Dobbs, Marc Wasmuth, John Wolff, Erica Carlson, Mary Fujimoto, Esther Krapcho, Karen Sears, Tena Woodward, Scott Hughes, J. Burt, Randy Gardner, Eldon Lalouel, Jean-Marc White, Ray
Citation: Nakamura, Yusuke et al., Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5, American journal of human genetics , 43-II(5), 1988, pp. 638-644
Compound heterozygote for lipoprotein lipase deficiency: Ser----Thr244 and transition in 3' splice site of intron 2 (AG----AA) in the lipoprotein lipase gene.
Authors: Hata, Akira Emi, Mitsuru Luc, Gerald Basdevant, Alain Gambert, Philippe Iverius, Per-Henrik Lalouel, Jean-Marc
Citation: Hata, Akira et al., Compound heterozygote for lipoprotein lipase deficiency: Ser----Thr244 and transition in 3' splice site of intron 2 (AG----AA) in the lipoprotein lipase gene., American journal of human genetics , 47-II(4), 1990, pp. 721-726
Localization of the genetic defect in multiple endocrine neoplasia type i within a small region of chromosome Il
Authors: Nakamura, Yusuke Larson, Catharina Julier, Cecile Byström, Camilla Skogseid, Britt Wells, Samuel Öberg, Kjell Carlson, Mary Taggart, Thomas O'Connell, Peter Leppert, Mark Lalouel, Jean-Marc Nordenskjöld, Magnus White, Ray
Citation: Nakamura, Yusuke et al., Localization of the genetic defect in multiple endocrine neoplasia type i within a small region of chromosome Il, American journal of human genetics , 44(5), 1989, pp. 751-755
Natural Selection and Population History in the Human Angiotensinogen Gene (AGT): 736 Complete AGT Sequences in Chromosomes from Around the World
Authors: Nakajima, Toshiaki Wooding, Stephen Sakagami, Takuro Emi, Mitsuru Tokunaga, Katsushi Tamiya, Gen Ishigami, Tomoaki Umemura, Satoshi Munkhbat, Batmunkh Jin, Feng Guan-jun, Jia Hayasaka, Ikuo Ishida, Takafumi Saitou, Naruya Pavelka, Karel Lalouel, Jean-Marc Jorde, Lynn B. Inoue, Ituro
Citation: Nakajima, Toshiaki et al., Natural Selection and Population History in the Human Angiotensinogen Gene (AGT): 736 Complete AGT Sequences in Chromosomes from Around the World, American journal of human genetics , 74(5), 2004, pp. 898-916
Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).
Authors: Chance, Phillip F. Bird, Thomas D. O'Connell, Peter Lipe, Hillary Lalouel, Jean-Marc Leppert, Mark
Citation: F. Chance, Phillip et al., Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I)., American journal of human genetics , 47-II(6), 1990, pp. 915-925
Etiological heterogeneity in X-linked spastic paraplegia
Authors: Keppen, Laura D. Leppert, Mark F. O'Connell, Peter Nakamura, Yusuke Stauffer, Dora Lathrop, Mark Lalouel, Jean-Marc White, Ray
Citation: D. Keppen, Laura et al., Etiological heterogeneity in X-linked spastic paraplegia, American journal of human genetics , 41-II(5), 1987, pp. 933-943
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