Fain P - Search Results

1

A genomic search for linkage of neurofibromatosis to RFLPs.

Barker D, Wright E, Nguyen K, Cannon L, Fain P, Goldgar D, Bishop DT, Carey J, Kivlin J, Willard H, et al. Barker D, et al. Among authors: fain p. J Med Genet. 1987 Sep;24(9):536-8. doi: 10.1136/jmg.24.9.536. J Med Genet. 1987. PMID: 2889831 Free PMC article.

2

Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?

Stern HJ, Saal HM, Lee JS, Fain PR, Goldgar DE, Rosenbaum KN, Barker DF. Stern HJ, et al. Among authors: fain pr. J Med Genet. 1992 Mar;29(3):184-7. doi: 10.1136/jmg.29.3.184. J Med Genet. 1992. PMID: 1348094 Free PMC article.

3

High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers.

Barker DF, Fain PR, Goldgar DE, Dietz-Band JN, Turco AE, Kashtan CE, Gregory MC, Tryggvason K, Skolnick MH, Atkin CL. Barker DF, et al. Among authors: fain pr. Hum Genet. 1991 Dec;88(2):189-94. doi: 10.1007/BF00206070. Hum Genet. 1991. PMID: 1684566

4

The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpoints.

Fain PR, Wright E, Willard HF, Stephens K, Barker DF. Fain PR, et al. Am J Hum Genet. 1989 Jan;44(1):68-72. Am J Hum Genet. 1989. PMID: 2491785 Free PMC article.

5

Refined physical and genetic mapping of the NF1 region on chromosome 17.

Fain PR, Goldgar DE, Wallace MR, Collins FS, Wright E, Nguyen K, Barker DF. Fain PR, et al. Am J Hum Genet. 1989 Nov;45(5):721-8. Am J Hum Genet. 1989. PMID: 2573276 Free PMC article.

6

Genetic analysis of NF1: identification of close flanking markers on chromosome 17.

Fain PR, Barker DF, Goldgar DE, Wright E, Nguyen K, Carey J, Johnson J, Kivlin J, Willard H, Mathew C, et al. Fain PR, et al. Genomics. 1987 Dec;1(4):340-5. doi: 10.1016/0888-7543(87)90034-6. Genomics. 1987. PMID: 3130304

7

Models of multilocus recombination: nonrandomness in chiasma number and crossover positions.

Goldgar DE, Fain PR. Goldgar DE, et al. Among authors: fain pr. Am J Hum Genet. 1988 Jul;43(1):38-45. Am J Hum Genet. 1988. PMID: 3163889 Free PMC article.

8

A 2D crossover-based map of the human X chromosome as a model for map integration.

Fain PR, Kort EN, Chance PF, Nguyen K, Redd DF, Econs MJ, Barker DF. Fain PR, et al. Nat Genet. 1995 Mar;9(3):261-6. doi: 10.1038/ng0395-261. Nat Genet. 1995. PMID: 7773289

9

Two simple repeat polymorphisms at DXS337.

Barker DF, Nguyen K, Fain PR. Barker DF, et al. Among authors: fain pr. Hum Mol Genet. 1993 Sep;2(9):1507. Hum Mol Genet. 1993. PMID: 8242086 No abstract available.

10

Refined genetic mapping of X-linked Charcot-Marie-Tooth neuropathy.

Fain PR, Barker DF, Chance PF. Fain PR, et al. Am J Hum Genet. 1994 Feb;54(2):229-35. Am J Hum Genet. 1994. PMID: 8304339 Free PMC article.

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