Willard H - 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: willard h. 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

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. Among authors: willard h. Genomics. 1987 Dec;1(4):340-5. doi: 10.1016/0888-7543(87)90034-6. Genomics. 1987. PMID: 3130304

3

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. Among authors: willard hf. Am J Hum Genet. 1989 Jan;44(1):68-72. Am J Hum Genet. 1989. PMID: 2491785 Free PMC article.

4

Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers.

Dietz-Band JN, Turco AE, Willard HF, Vincent A, Skolnick MH, Barker DF. Dietz-Band JN, et al. Among authors: willard hf. Cytogenet Cell Genet. 1990;54(3-4):137-41. doi: 10.1159/000132977. Cytogenet Cell Genet. 1990. PMID: 1979940

5

Genetic analysis of eight loci tightly linked to neurofibromatosis 1.

Stephens K, Green P, Riccardi VM, Ng S, Rising M, Barker D, Darby JK, Falls KM, Collins FS, Willard HF, et al. Stephens K, et al. Among authors: willard hf. Am J Hum Genet. 1989 Jan;44(1):13-9. Am J Hum Genet. 1989. PMID: 2491775 Free PMC article.

6

Genetic linkage map of human chromosome 7 with 63 DNA markers.

Barker D, Green P, Knowlton R, Schumm J, Lander E, Oliphant A, Willard H, Akots G, Brown V, Gravius T, et al. Barker D, et al. Among authors: willard h. Proc Natl Acad Sci U S A. 1987 Nov;84(22):8006-10. doi: 10.1073/pnas.84.22.8006. Proc Natl Acad Sci U S A. 1987. PMID: 2891136 Free PMC article.

7

Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome.

Lafrenière RG, Brown CJ, Powers VE, Carrel L, Davies KE, Barker DF, Willard HF. Lafrenière RG, et al. Among authors: willard hf. Genomics. 1991 Oct;11(2):352-63. doi: 10.1016/0888-7543(91)90143-3. Genomics. 1991. PMID: 1685139

8

Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction.

Greer WL, Mahtani MM, Kwong PC, Rubin LA, Peacocke M, Willard HF, Siminovitch KA. Greer WL, et al. Among authors: willard hf. Hum Genet. 1989 Oct;83(3):227-30. doi: 10.1007/BF00285161. Hum Genet. 1989. PMID: 2571560

9

Molecular organization and haplotype analysis of centromeric DNA from human chromosome 17: implications for linkage in neurofibromatosis.

Willard HF, Greig GM, Powers VE, Waye JS. Willard HF, et al. Genomics. 1987 Dec;1(4):368-73. doi: 10.1016/0888-7543(87)90041-3. Genomics. 1987. PMID: 2896633

10

A centromere-based linkage group on the long arm of human chromosome 17.

Tsipouras P, Schwartz RC, Phillips JA 3rd, Willard HF. Tsipouras P, et al. Among authors: willard hf. Cytogenet Cell Genet. 1988;47(1-2):109-10. doi: 10.1159/000132523. Cytogenet Cell Genet. 1988. PMID: 3162714

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