Willard HF - Search Results

1

Uniparental disomy as a mechanism for human genetic disease.

Spence JE, Perciaccante RG, Greig GM, Willard HF, Ledbetter DH, Hejtmancik JF, Pollack MS, O'Brien WE, Beaudet AL. Spence JE, et al. Among authors: willard hf. Am J Hum Genet. 1988 Feb;42(2):217-26. Am J Hum Genet. 1988. PMID: 2893543 Free PMC article.

2

Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16.

Greig GM, England SB, Bedford HM, Willard HF. Greig GM, et al. Among authors: willard hf. Am J Hum Genet. 1989 Dec;45(6):862-72. Am J Hum Genet. 1989. PMID: 2573999 Free PMC article.

3

Detection of novel centromeric polymorphisms associated with alpha satellite DNA from human chromosome 11.

Waye JS, Greig GM, Willard HF. Waye JS, et al. Among authors: willard hf. Hum Genet. 1987 Oct;77(2):151-6. doi: 10.1007/BF00272383. Hum Genet. 1987. PMID: 2888719

4

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

5

Duplicated zinc finger protein genes on the proximal short arm of the human X chromosome: isolation, characterization and X-inactivation studies.

Greig GM, Sharp CB, Carrel L, Willard HF. Greig GM, et al. Among authors: willard hf. Hum Mol Genet. 1993 Oct;2(10):1611-8. doi: 10.1093/hmg/2.10.1611. Hum Mol Genet. 1993. PMID: 8268913

6

Organization and evolution of an alpha satellite DNA subset shared by human chromosomes 13 and 21.

Greig GM, Warburton PE, Willard HF. Greig GM, et al. Among authors: willard hf. J Mol Evol. 1993 Nov;37(5):464-75. doi: 10.1007/BF00160427. J Mol Evol. 1993. PMID: 8283478

7

PCR amplification of chromosome-specific alpha satellite DNA: definition of centromeric STS markers and polymorphic analysis.

Warburton PE, Greig GM, Haaf T, Willard HF. Warburton PE, et al. Among authors: willard hf. Genomics. 1991 Oct;11(2):324-33. doi: 10.1016/0888-7543(91)90139-6. Genomics. 1991. PMID: 1685138

8

Five polymorphic microsatellite VNTRs on the human X chromosome.

Luty JA, Guo Z, Willard HF, Ledbetter DH, Ledbetter S, Litt M. Luty JA, et al. Among authors: willard hf. Am J Hum Genet. 1990 Apr;46(4):776-83. Am J Hum Genet. 1990. PMID: 2316523 Free PMC article.

9

Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM.

Bascom RA, García-Heras J, Hsieh CL, Gerhard DS, Jones C, Francke U, Willard HF, Ledbetter DH, McInnes RR. Bascom RA, et al. Among authors: willard hf. Am J Hum Genet. 1992 Nov;51(5):1028-35. Am J Hum Genet. 1992. PMID: 1415249 Free PMC article.

10

Molecular cytogenetics of alpha satellite DNA from chromosome 12: fluorescence in situ hybridization and description of DNA and array length polymorphisms.

Greig GM, Parikh S, George J, Powers VE, Willard HF. Greig GM, et al. Among authors: willard hf. Cytogenet Cell Genet. 1991;56(3-4):144-8. doi: 10.1159/000133071. Cytogenet Cell Genet. 1991. PMID: 1675980

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