Leppert M - Search Results

1

Genetic linkage of Paget disease of the bone to chromosome 18q.

Cody JD, Singer FR, Roodman GD, Otterund B, Lewis TB, Leppert M, Leach RJ. Cody JD, et al. Among authors: leppert m. Am J Hum Genet. 1997 Nov;61(5):1117-22. doi: 10.1086/301601. Am J Hum Genet. 1997. PMID: 9345096 Free PMC article.

2

Genetic linkage of the dentinogenesis imperfecta type III locus to chromosome 4q.

MacDougall M, Jeffords LG, Gu TT, Knight CB, Frei G, Reus BE, Otterud B, Leppert M, Leach RJ. MacDougall M, et al. Among authors: leppert m. J Dent Res. 1999 Jun;78(6):1277-82. doi: 10.1177/00220345990780061301. J Dent Res. 1999. PMID: 10371253

3

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.

Charlier C, Singh NA, Ryan SG, Lewis TB, Reus BE, Leach RJ, Leppert M. Charlier C, et al. Among authors: leppert m. Nat Genet. 1998 Jan;18(1):53-5. doi: 10.1038/ng0198-53. Nat Genet. 1998. PMID: 9425900

4

A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p.

Anderson KL, Baird L, Lewis RA, Chinault AC, Otterud B, Leppert M, Lupski JR. Anderson KL, et al. Among authors: leppert m. Am J Hum Genet. 1995 Dec;57(6):1351-63. Am J Hum Genet. 1995. PMID: 8533764 Free PMC article.

5

Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigrees.

Katsanis N, Lewis RA, Stockton DW, Mai PM, Baird L, Beales PL, Leppert M, Lupski JR. Katsanis N, et al. Among authors: leppert m. Am J Hum Genet. 1999 Dec;65(6):1672-9. doi: 10.1086/302684. Am J Hum Genet. 1999. PMID: 10577921 Free PMC article.

6

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.

Singh NA, Charlier C, Stauffer D, DuPont BR, Leach RJ, Melis R, Ronen GM, Bjerre I, Quattlebaum T, Murphy JV, McHarg ML, Gagnon D, Rosales TO, Peiffer A, Anderson VE, Leppert M. Singh NA, et al. Among authors: leppert m. Nat Genet. 1998 Jan;18(1):25-9. doi: 10.1038/ng0198-25. Nat Genet. 1998. PMID: 9425895

7

Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q.

Fink JK, Rainer S, Wilkowski J, Jones SM, Kume A, Hedera P, Albin R, Mathay J, Girbach L, Varvil T, Otterud B, Leppert M. Fink JK, et al. Among authors: leppert m. Am J Hum Genet. 1996 Jul;59(1):140-5. Am J Hum Genet. 1996. PMID: 8659518 Free PMC article.

8

Genetic heterogeneity in familial acute myelogenous leukemia: evidence for a second locus at chromosome 16q21-23.2.

Horwitz M, Benson KF, Li FQ, Wolff J, Leppert MF, Hobson L, Mangelsdorf M, Yu S, Hewett D, Richards RI, Raskind WH. Horwitz M, et al. Among authors: leppert mf. Am J Hum Genet. 1997 Oct;61(4):873-81. doi: 10.1086/514894. Am J Hum Genet. 1997. PMID: 9382098 Free PMC article.

9

Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity.

Heath H 3rd, Jackson CE, Otterud B, Leppert MF. Heath H 3rd, et al. Among authors: leppert mf. Am J Hum Genet. 1993 Jul;53(1):193-200. Am J Hum Genet. 1993. PMID: 8317484 Free PMC article.

10

A primary genetic map of chromosome 13q.

Leppert M, Cavenee W, Callahan P, Holm T, O'Connell P, Thompson K, Lathrop GM, Lalouel JM, White R. Leppert M, et al. Am J Hum Genet. 1986 Oct;39(4):425-37. Am J Hum Genet. 1986. PMID: 3464200 Free PMC article.

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