O'Connell P - Search Results

1

A breast-ovarian cancer susceptibility gene maps to chromosome 17q21.

Feunteun J, Narod SA, Lynch HT, Watson P, Conway T, Lynch J, Parboosingh J, O'Connell P, White R, Lenoir GM. Feunteun J, et al. Am J Hum Genet. 1993 Apr;52(4):736-42. Am J Hum Genet. 1993. PMID: 8460639 Free PMC article.

2

Identification and characterization of the gene for neurofibromatosis type 1.

White R, O'Connell P. White R, et al. Curr Opin Genet Dev. 1991 Jun;1(1):15-9. doi: 10.1016/0959-437x(91)80034-j. Curr Opin Genet Dev. 1991. PMID: 1840873 Review.

3

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.

4

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

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

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.

7

A radiation hybrid map of the BRCA1 region.

O'Connell P, Albertsen H, Matsunami N, Taylor T, Hundley JE, Johnson-Pais TL, Reus B, Lawrence E, Ballard L, White R, et al. O'Connell P, et al. Am J Hum Genet. 1994 Mar;54(3):526-34. Am J Hum Genet. 1994. PMID: 8116622 Free PMC article.

8

Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17.

Fountain JW, Wallace MR, Brereton AM, O'Connell P, White RL, Rich DC, Ledbetter DH, Leach RJ, Fournier RE, Menon AG, et al. Fountain JW, et al. Am J Hum Genet. 1989 Jan;44(1):58-67. Am J Hum Genet. 1989. PMID: 2491783 Free PMC article.

9

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.

10

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. Am J Hum Genet. 1987 Nov;41(5):933-43. Am J Hum Genet. 1987. PMID: 3479019 Free PMC article.

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