MeSH Treeview
Query OMIM entry list
602929
LOH11CR2A
LOSS OF HETEROZYGOSITY, CHROMOSOME 11, REGION 2, GENE A
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Metabolic Phenomena
Pharmacokinetics
Tissue Distribution
Genetic Phenomena
Genetic Processes
Mutagenesis
Translocation, Genetic
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 12
Genome
Genome Components
Genes
Genes, Neoplasm
Genes, Tumor Suppressor
Genes, Recessive
Genes, Tumor Suppressor
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Aberrations
Translocation, Genetic
Polymorphism, Genetic
Polymorphism, Single-Stranded Conformational
Genotype
Heterozygote
Physiological Phenomena
Pharmacological Phenomena
Pharmacokinetics
Tissue Distribution
Database Center for Life Science
