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A Genetic Map of the Mouse Suitable for Typing Intraspecific Crosses

Genetics (Austin), 1992-06, Vol.131 (2), p.423-447

1992

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Progress in high throughput SNP genotyping methods

The pharmacogenomics journal, 2002, Vol.2 (2), p.103-110

2002

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Germline p16 mutations in familial melanoma

Nature genetics, 1994-09, Vol.8 (1), p.15-21

1994

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Loss of Heterozygosity for the Short Arm of Chromosome 1 in Human Neuroblastomas: Correlation with N-myc Amplification

Proceedings of the National Academy of Sciences - PNAS, 1989-05, Vol.86 (10), p.3753-3757

1989

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Homozygous Deletions within Human Chromosome Band 9p21 in Melanoma

Proceedings of the National Academy of Sciences - PNAS, 1992-11, Vol.89 (21), p.10557-10561

1992

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Linkage of cutaneous malignant melanoma/dysplastic nevi to chromosome 9p, and evidence for genetic heterogeneity

American journal of human genetics, 1994-03, Vol.54 (3), p.489-496

1994

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Loss of Alleles from the Distal Short Arm of Chromosome 1 Occurs Late in Melanoma Tumor Progression

Proceedings of the National Academy of Sciences - PNAS, 1989-06, Vol.86 (12), p.4614-4618

1989

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Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms

Genomics (San Diego, Calif.), 1992-07, Vol.13 (3), p.622-629

1992

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Sun-Related Risk Factors in Melanoma-Prone Families With CDKN2A Mutations

JNCI : Journal of the National Cancer Institute, 1998-05, Vol.90 (9), p.709-711

1998

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Two-locus linkage analysis of cutaneous malignant melanoma/dysplastic nevi

American journal of human genetics, 1996-05, Vol.58 (5), p.1050-1056

1996

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Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus to chromosome 1p

The New England journal of medicine, 1989-05, Vol.320 (21), p.1367

1989

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Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19

American journal of human genetics, 1993-11, Vol.53 (5), p.1079-1095

1993

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Pluripotent embryonal carcinoma clones derived from the human teratocarcinoma cell line Tera-2. Differentiation in vivo and in vitro

Laboratory investigation, 1984-02, Vol.50 (2), p.147

1984

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Familial hypothyroidism caused by a nonsense mutation in the thyroid-stimulating hormone β-subunit gene

American journal of human genetics, 1990-05, Vol.46 (5), p.988-993

1990

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Restoration of CDKN2A into Melanoma Cells Induces Morphologic Changes and Reduction in Growth Rate but Not Anchorage-Independent Growth Reversal

Journal of investigative dermatology, 1997-07, Vol.109 (1), p.61-68

1997

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Loss of Polymorphic Restriction Fragments in Malignant Melanoma: Implications for Tumor Heterogeneity

Proceedings of the National Academy of Sciences - PNAS, 1985-03, Vol.82 (5), p.1470-1474

1985

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Development of oncology drug response markers using transcription profiling

Current molecular medicine, 2005-02, Vol.5 (1), p.103-110

Dracopoli, Nicholas C

2005

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Identification of a new murine runt domain-containing gene, Cbfa3, and localization of the human homolog, CBFA3, to chromosome 1p35-pter

Genomics (San Diego, Calif.), 1995-04, Vol.26 (3), p.611-614

1995

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Mutations of the p16 gene product are rare in prostate cancer

The Prostate, 1997-02, Vol.30 (3), p.188-194

1997

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A PCR-Based Linkage Map of Human Chromosome 1

Genomics (San Diego, Calif.), 1993-02, Vol.15 (2), p.251-258

1993

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Genetic and physical map of the interferon region on chromosome 9p

Genomics (San Diego, Calif.), 1992-09, Vol.14 (1), p.105-112

1992

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Loss of heterozygosity at autosomal and X-linked loci during tumor progression in a patient with melanoma

Cancer research (Chicago, Ill.), 1987-08, Vol.47 (15), p.3995-4000

1987

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Somatic Cell Genetic Analysis of Human Cell Surface Antigens: Chromosomal Assignments and Regulation of Expression in Rodent--Human Hybrid Cells

Proceedings of the National Academy of Sciences - PNAS, 1984-10, Vol.81 (20), p.6437-6441

1984

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Evidence against Ha- ras -1 involvement in sporadic and familial melanoma

Nature (London), 1987-01, Vol.325 (6099), p.73-75

1987

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Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell lines

Nature genetics, 1993-02, Vol.3 (2), p.118-121

1993

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A Genetic Map of the Mouse Suitable for Typing Intraspecific Crosses

Progress in high throughput SNP genotyping methods

Germline p16 mutations in familial melanoma

Loss of Heterozygosity for the Short Arm of Chromosome 1 in Human Neuroblastomas: Correlation with N-myc Amplification

Homozygous Deletions within Human Chromosome Band 9p21 in Melanoma

Linkage of cutaneous malignant melanoma/dysplastic nevi to chromosome 9p, and evidence for genetic heterogeneity

Loss of Alleles from the Distal Short Arm of Chromosome 1 Occurs Late in Melanoma Tumor Progression

Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms

Sun-Related Risk Factors in Melanoma-Prone Families With CDKN2A Mutations

Two-locus linkage analysis of cutaneous malignant melanoma/dysplastic nevi

Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus to chromosome 1p

Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19

Pluripotent embryonal carcinoma clones derived from the human teratocarcinoma cell line Tera-2. Differentiation in vivo and in vitro

Familial hypothyroidism caused by a nonsense mutation in the thyroid-stimulating hormone β-subunit gene

Restoration of CDKN2A into Melanoma Cells Induces Morphologic Changes and Reduction in Growth Rate but Not Anchorage-Independent Growth Reversal

Loss of Polymorphic Restriction Fragments in Malignant Melanoma: Implications for Tumor Heterogeneity

Development of oncology drug response markers using transcription profiling

Identification of a new murine runt domain-containing gene, Cbfa3, and localization of the human homolog, CBFA3, to chromosome 1p35-pter

Mutations of the p16 gene product are rare in prostate cancer

A PCR-Based Linkage Map of Human Chromosome 1

Genetic and physical map of the interferon region on chromosome 9p

Loss of heterozygosity at autosomal and X-linked loci during tumor progression in a patient with melanoma

Somatic Cell Genetic Analysis of Human Cell Surface Antigens: Chromosomal Assignments and Regulation of Expression in Rodent--Human Hybrid Cells

Evidence against Ha- ras -1 involvement in sporadic and familial melanoma

Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell lines

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