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The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome.
Vincent GM, Timothy KW, Leppert M, Keating M. Vincent GM, et al. Among authors: leppert m. N Engl J Med. 1992 Sep 17;327(12):846-52. doi: 10.1056/NEJM199209173271204. N Engl J Med. 1992. PMID: 1508244
Twenty loci form a continuous linkage map of markers for human chromosome 2.
O'Connell P, Lathrop GM, Nakamura Y, Leppert ML, Lalouel JM, White R. O'Connell P, et al. Among authors: leppert ml. Genomics. 1989 Nov;5(4):738-45. doi: 10.1016/0888-7543(89)90115-8. Genomics. 1989. PMID: 2591961
Twenty-eight loci form a continuous linkage map of markers for human chromosome 1.
O'Connell P, Lathrop GM, Nakamura Y, Leppert ML, Ardinger RH, Murray JL, Lalouel JM, White R. O'Connell P, et al. Among authors: leppert ml. Genomics. 1989 Jan;4(1):12-20. doi: 10.1016/0888-7543(89)90308-x. Genomics. 1989. PMID: 2914706
Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p.
Gouw LG, Kaplan CD, Haines JH, Digre KB, Rutledge SL, Matilla A, Leppert M, Zoghbi HY, Ptácek LJ. Gouw LG, et al. Among authors: leppert m. Nat Genet. 1995 May;10(1):89-93. doi: 10.1038/ng0595-89. Nat Genet. 1995. PMID: 7647799
A primary map of 24 loci on human chromosome 16.
Julier C, Nakamura Y, Lathrop M, O'Connell P, Leppert M, Mohandas T, Lalouel JM, White R. Julier C, et al. Among authors: leppert m. Genomics. 1990 Mar;6(3):419-27. doi: 10.1016/0888-7543(90)90471-6. Genomics. 1990. PMID: 2328986
Linkage analysis of schizophrenia: the D1 dopamine receptor gene and several flanking DNA markers.
Jensen S, Plaetke R, Holik J, Hoff M, Myles-Worsley M, Leppert M, Coon H, Vest K, Freedman R, Waldo M, et al. Jensen S, et al. Among authors: leppert m. Hum Hered. 1993 Jan-Feb;43(1):58-62. doi: 10.1159/000154115. Hum Hered. 1993. PMID: 8514328
Genomic scan for genes predisposing to schizophrenia.
Coon H, Jensen S, Holik J, Hoff M, Myles-Worsley M, Reimherr F, Wender P, Waldo M, Freedman R, Leppert M, et al. Coon H, et al. Among authors: leppert m. Am J Med Genet. 1994 Mar 15;54(1):59-71. doi: 10.1002/ajmg.1320540111. Am J Med Genet. 1994. PMID: 7909992
A mapped set of genetic markers for human chromosome 9.
Lathrop M, Nakamura Y, O'Connell P, Leppert M, Woodward S, Lalouel JM, White R. Lathrop M, et al. Among authors: leppert m. Genomics. 1988 Nov;3(4):361-6. doi: 10.1016/0888-7543(88)90128-0. Genomics. 1988. PMID: 3243551
Benign familial neonatal convulsions linked to genetic markers on chromosome 20.
Leppert M, Anderson VE, Quattlebaum T, Stauffer D, O'Connell P, Nakamura Y, Lalouel JM, White R. Leppert M, et al. Nature. 1989 Feb 16;337(6208):647-8. doi: 10.1038/337647a0. Nature. 1989. PMID: 2918897
An extended genetic linkage map of markers for human chromosome 10.
Nakamura Y, Lathrop M, Bragg T, Leppert M, O'Connell P, Jones C, Lalouel JM, White R. Nakamura Y, et al. Among authors: leppert m. Genomics. 1988 Nov;3(4):389-92. doi: 10.1016/0888-7543(88)90133-4. Genomics. 1988. PMID: 2907505
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