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Genome-wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early-onset major depression and anxiety disorders

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2005-05, Vol.135B (1), p.85-93

2005

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Common inheritance of susceptibility to colonic adenomatous polyps and associated colorectal cancers

The New England journal of medicine, 1988-09, Vol.319 (9), p.533-537

1988

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Association of common missense changes in ELAC2 ( HPC2) with prostate cancer in a Japanese case-control series

Journal of human genetics, 2002-01, Vol.47 (12), p.641-648

2002

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Rates of p16 (MTS1) Mutations in Primary Tumors with 9p Loss

Science (American Association for the Advancement of Science), 1994-07, Vol.265 (5170), p.415-417

1994

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Assignment of a Locus for Familial Melanoma, MLM, to Chromosome 9p13-p22

Science (American Association for the Advancement of Science), 1992-11, Vol.258 (5085), p.1148-1152

1992

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Localization of a Putative Tumor Suppressor Gene by Using Homozygous Deletions in Melanomas

Proceedings of the National Academy of Sciences - PNAS, 1994-08, Vol.91 (16), p.7563-7567

1994

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Hereditary hemochromatosis. Analysis of laboratory expression of the disease by genotype in 18 pedigrees

American journal of clinical pathology, 1982-08, Vol.78 (2), p.196-207

1982

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A probabilistic model for detecting coding regions in DNA sequences

Mathematical medicine and biology, 1994, Vol.11 (3), p.149-160

1994

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Global fractal dimension of human DNA sequences treated as pseudorandom walks

Physical review. A, Atomic, molecular, and optical physics, 1992-06, Vol.45 (12), p.8902-8913

1992

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BRCA1 germline mutational spectrum in Italian families from Tuscany: a high frequency of novel mutations

Oncogene, 1996-10, Vol.13 (7), p.1483-1488

1996

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Prevalence of hemochromatosis

The New England journal of medicine, 1988-12, Vol.319 (23), p.1548-1549

1988

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Common inheritance of susceptibility to colonic adenomatous polyps and associated colorectal cancers

The New England journal of medicine, 1989-02, Vol.320 (5), p.316-317

1989

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Mutations in the BRCA1 gene in Japanese breast cancer patients

Human mutation, 1996, Vol.7 (4), p.334-339

1996

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A screening study of prostate cancer in high risk families

The Journal of urology, 1992-09, Vol.148 (3), p.826-827

1992

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Genomic mismatch scanning in pedigrees

Mathematical medicine and biology, 1994, Vol.11 (1), p.1-16

1994

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Response : Rates of p16 ( MTS1 ) Mutations in Primary Tumors with 9p Loss

Science (American Association for the Advancement of Science), 1994-07, Vol.265 (5170), p.416-417

1994

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Automatic program generation for processing a high level relational-like query language

ACM Annual Conference/Annual Meeting: Proceedings of the 1979 annual conference, 1979, p.62-68

1979

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Title Page / Table of Contents

Cytogenetic and genome research, 1992, Vol.59 (2-3), p.65-73

1992

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Generation of an Integrated Transcription Map of theBRCA2Region on Chromosome 13q12–q13

Genomics (San Diego, Calif.), 1996-08, Vol.36 (1), p.86-99

1996

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Coincidental Nontransfusional Iron Overload and Thalassemia Minor: Association With HLA-Linked Hemochromatosis

Blood, 1981-10, Vol.58 (4), p.844-848

1981

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Screening for Hemochromatosis in Healthy Blood Donors

Annals of the New York Academy of Sciences, 1988-06, Vol.526 (1), p.258-273

1988

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Sporadic Porphyria Cutanea Tarda in Individuals with HLA-linked Hemochromatosis Allele(s)

Annals of the New York Academy of Sciences, 1988-06, Vol.526 (1), p.47-53

1988

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Histopathologic characteristics of dysplastic nevi

Journal of the American Academy of Dermatology, 1990-05, Vol.22 (5), p.727-733

1990

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Inheritance of proliferative breast disease in breast cancer kindred

Science (American Association for the Advancement of Science), 1990-12, Vol.250 (4988), p.1715

1990

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Iron overload in hereditary spherocytosis: Association with hla‐linked hemochromatosis

American journal of hematology, 1982-09, Vol.13 (2), p.101-109

1982

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Genome-wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early-onset major depression and anxiety disorders

Common inheritance of susceptibility to colonic adenomatous polyps and associated colorectal cancers

Association of common missense changes in ELAC2 ( HPC2) with prostate cancer in a Japanese case-control series

Rates of p16 (MTS1) Mutations in Primary Tumors with 9p Loss

Assignment of a Locus for Familial Melanoma, MLM, to Chromosome 9p13-p22

Localization of a Putative Tumor Suppressor Gene by Using Homozygous Deletions in Melanomas

Hereditary hemochromatosis. Analysis of laboratory expression of the disease by genotype in 18 pedigrees

A probabilistic model for detecting coding regions in DNA sequences

Global fractal dimension of human DNA sequences treated as pseudorandom walks

BRCA1 germline mutational spectrum in Italian families from Tuscany: a high frequency of novel mutations

Prevalence of hemochromatosis

Common inheritance of susceptibility to colonic adenomatous polyps and associated colorectal cancers

Mutations in the BRCA1 gene in Japanese breast cancer patients

A screening study of prostate cancer in high risk families

Genomic mismatch scanning in pedigrees

Response : Rates of p16 ( MTS1 ) Mutations in Primary Tumors with 9p Loss

Automatic program generation for processing a high level relational-like query language

Title Page / Table of Contents

Generation of an Integrated Transcription Map of theBRCA2Region on Chromosome 13q12–q13

Coincidental Nontransfusional Iron Overload and Thalassemia Minor: Association With HLA-Linked Hemochromatosis

Screening for Hemochromatosis in Healthy Blood Donors

Sporadic Porphyria Cutanea Tarda in Individuals with HLA-linked Hemochromatosis Allele(s)

Histopathologic characteristics of dysplastic nevi

Inheritance of proliferative breast disease in breast cancer kindred

Iron overload in hereditary spherocytosis: Association with hla‐linked hemochromatosis

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