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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 3/2001, Volume 98, Issue 6, pp. 3387 - 3392
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2008, Volume 3, Issue 10, pp. e3519 - e3519
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 2, pp. e16747 - e16747
Journal Article
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 04/2010, Volume 18, Issue 4, pp. 471 - 478
Journal Article
Nature Genetics, ISSN 1061-4036, 04/2002, Volume 30, Issue 4, pp. 406 - 410
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 07/1994, Volume 331, Issue 4, pp. 213 - 221
Journal Article
Science, ISSN 0036-8075, 5/1993, Volume 260, Issue 5109, pp. 812 - 816
A predisposition to colorectal cancer is shown to be linked to markers on chromosome 2 in some families. Molecular features of "familial" cancers were compared... 
Colorectal cancer | Alleles | Microsatellite repeats | Loss of heterozygosity | Tumor suppressor genes | Reports | Hereditary nonpolyposis colorectal neoplasms | Genetic mutation | Chromosomes | Tumors | Cancer | ONCOGENES | TUMOR SUPPRESSOR GENES | MULTIDISCIPLINARY SCIENCES | CARCINOMAS | CHROMOSOME-5Q21 | MUTATIONS | IDENTIFICATION | TUMORIGENESIS | EXPRESSION | LOCUS | P53 | Colonic Neoplasms - genetics | Colorectal Neoplasms - genetics | Humans | Male | Chromosome Mapping | Genetic Markers | Lod Score | Polymorphism, Genetic | Chromosomes, Human, Pair 2 | Rectal Neoplasms - genetics | Pedigree | Repetitive Sequences, Nucleic Acid | DNA, Satellite - genetics | Female | Mutation | Satellite DNA | Genetic disorders | Medical genetics | Causes of | Research | Genetic screening | Genes | Colon cancer | tumor suppressor genes | colorectal | carcinoma | chromosome 2 | man | tumorigenesis | colorectal carcinoma | analysis | Index Medicus | LARGE INTESTINE | GASTROINTESTINAL TRACT | ERRORS | DIGESTIVE SYSTEM | GENOME MUTATIONS | BIOLOGICAL MARKERS | 550400 - Genetics | DNA REPLICATION | MAPPING | HUMAN CHROMOSOMES | HUMAN POPULATIONS | NEOPLASMS | BASIC BIOLOGICAL SCIENCES | POPULATIONS | HYBRIDIZATION | INTESTINES | CHROMOSOMES | HUMAN CHROMOSOME 2 | ORGANS | DISEASES | NUCLEIC ACID REPLICATION | GENETIC MAPPING | DNA HYBRIDIZATION | BODY | RFLPS
Journal Article
Journal Article
Investigative Ophthalmology & Visual Science, ISSN 0146-0404, 10/2002, Volume 43, Issue 10, pp. 3160 - 3164
PURPOSE. The estimated world-wide prevalence of keratoconus is 50 to 230 per 100,000 in the general population. Sporadic keratoconus is the leading cause of... 
OPHTHALMOLOGY | LCAT | MUTATIONS | GENE | DISEASE | Humans | Male | Chromosome Mapping | Lod Score | Genes, Dominant | Pedigree | Adolescent | Alleles | Finland | Keratoconus - genetics | Adult | Female | Chromosomes, Human, Pair 16 - genetics | Genetic Linkage | Index Medicus
Journal Article