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Query OMIM entry list
609625
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CHROMOSOME 10q DELETION SYNDROME
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Genetic Phenomena
Genetic Processes
Mutagenesis
Sequence Deletion
Chromosome Deletion
Translocation, Genetic
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 10
Ring Chromosomes
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Ring Chromosomes
Translocation, Genetic
Sequence Deletion
Chromosome Deletion
Phenotype
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
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