Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome

Human Molecular Genetics

Volumn 11, Issue 17, 2002, Pages 1987-1995

  Estivill, Xavier ^a,b,c   Cheung, Joseph ^a   Pujana, Miguel Angel ^b   Nakabayashi, Kazuhiko ^a   Scherer, Stephen W ^a   Tsui, Lap Chee ^a  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b Center for Genomic Regulation   (Spain)

^c HOSPITAL FOR SICK CHILDREN RESEARCH INSTITUTE   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME; CHROMOSOME 15Q; CHROMOSOME 17P; CHROMOSOME 22; CHROMOSOME 22Q; CHROMOSOME MAP; CONTROLLED STUDY; DATA ANALYSIS; DATA BASE; DENSITY; DEVICE; GENE DELETION; GENE DUPLICATION; GENE SEQUENCE; GENETIC DISORDER; HUMAN; HUMAN GENOME; NEUROFIBROMATOSIS; PERIPHERAL NEUROPATHY; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; BIOLOGY; CENTROMERE; CONTIG MAPPING; EXON; FACTUAL DATABASE; GENETICS; GENOME;

CENTROMERE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 22; COMPUTATIONAL BIOLOGY; CONTIG MAPPING; DATABASES, FACTUAL; EXONS; GENE DELETION; GENE DUPLICATION; GENOME, HUMAN; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 0037101840     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/11.17.1987     Document Type: Article

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