Leppert MF - Search Results

1

Etiological heterogeneity in X-linked spastic paraplegia.

Keppen LD, Leppert MF, O'Connell P, Nakamura Y, Stauffer D, Lathrop M, Lalouel JM, White R. Keppen LD, et al. Among authors: leppert mf. Am J Hum Genet. 1987 Nov;41(5):933-43. Am J Hum Genet. 1987. PMID: 3479019 Free PMC article.

2

Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).

Chance PF, Bird TD, O'Connell P, Lipe H, Lalouel JM, Leppert M. Chance PF, et al. Am J Hum Genet. 1990 Dec;47(6):915-25. Am J Hum Genet. 1990. PMID: 2239969 Free PMC article.

3

Linkage of DNA probe B79a (D7S13) to cystic fibrosis.

Wainwright BJ, Tsui LC, Leppert M, Buchwald M, Estivill X, O'Connell P, Lathrop M, Lalouel JM, White R, Williamson R, et al. Wainwright BJ, et al. Am J Hum Genet. 1987 Nov;41(5):944-7. Am J Hum Genet. 1987. PMID: 2890297 Free PMC article.

4

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.

5

A DNA probe for the LDL receptor gene is tightly linked to hypercholesterolemia in a pedigree with early coronary disease.

Leppert MF, Hasstedt SJ, Holm T, O'Connell P, Wu L, Ash O, Williams RR, White R. Leppert MF, et al. Am J Hum Genet. 1986 Sep;39(3):300-6. Am J Hum Genet. 1986. PMID: 2876626 Free PMC article.

6

Mapping approaches to gene identification in humans.

White RL, Lalouel JM, Lathrop GM, Leppert MF, Nakamura Y, O'Connell P. White RL, et al. Among authors: leppert mf. West J Med. 1987 Oct;147(4):423-7. West J Med. 1987. PMID: 3479870 Free PMC article.

7

Genetic linkage of the human gene for phenylethanolamine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21-q22.

Hoehe MR, Plaetke R, Otterud B, Stauffer D, Holik J, Byerley WF, Baetge EE, Gershon ES, Lalouel JM, Leppert M. Hoehe MR, et al. Hum Mol Genet. 1992 Jun;1(3):175-8. doi: 10.1093/hmg/1.3.175. Hum Mol Genet. 1992. PMID: 1303174

8

Diagnosis of neurofibromatosis I by using tightly linked, flanking DNA markers.

Ward K, O'Connell P, Carey JC, Leppert M, Jolley S, Plaetke R, Ogden B, White R. Ward K, et al. Am J Hum Genet. 1990 May;46(5):943-9. Am J Hum Genet. 1990. PMID: 1971145 Free PMC article.

9

R-banding and nonisotopic in situ hybridization: precise localization of the human type II collagen gene (COL2A1).

Takahashi E, Hori T, O'Connell P, Leppert M, White R. Takahashi E, et al. Hum Genet. 1990 Nov;86(1):14-6. doi: 10.1007/BF00205165. Hum Genet. 1990. PMID: 2253935

10

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. Genomics. 1990 Mar;6(3):419-27. doi: 10.1016/0888-7543(90)90471-6. Genomics. 1990. PMID: 2328986

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