Mapping of hereditary mixed polyposis syndrome (HMPS) to chromosome 10q23 by genomewide high-density single nucleotide polymorphism (SNP) scan and identification of BMPR1A loss of function.

Journal of medical genetics

Volumn 43, Issue 3, 2006, Pages

  Cao, X ^a   Eu, K W ^a   Kumarasinghe, M P ^a   Li, H H ^a   Loi, C ^a   Cheah, P Y ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

BMPR1A PROTEIN, HUMAN; BONE MORPHOGENETIC PROTEIN RECEPTOR 1; MICROSATELLITE DNA;

CHROMOSOME 10; CHROMOSOME MAP; COLON POLYPOSIS; COLORECTAL TUMOR; FEMALE; GENETICS; GENOME; GENOTYPE; HUMAN; LETTER; MALE; MUTATION; PEDIGREE; POLYMERASE CHAIN REACTION; SINGLE NUCLEOTIDE POLYMORPHISM;

ADENOMATOUS POLYPOSIS COLI; BONE MORPHOGENETIC PROTEIN RECEPTORS, TYPE I; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 10; COLORECTAL NEOPLASMS; FEMALE; GENOME, HUMAN; GENOTYPE; HUMANS; MALE; MICROSATELLITE REPEATS; MUTATION; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 33746806391     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2005.034827     Document Type: Letter

References (0)