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Query OMIM entry list
607872
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MONOSOMY 1p36 SYNDROME
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Sequence Homology
Sequence Homology, Amino Acid
Genetic Phenomena
Genetic Processes
DNA Damage
DNA Breaks
Chromosome Breakage
Gene Expression
Mutagenesis
Sequence Deletion
Chromosome Deletion
Gene Deletion
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 1
Genome
Genome Components
Genes
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosome Breakage
Sequence Deletion
Chromosome Deletion
Gene Deletion
Polymorphism, Genetic
Phenotype
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Sequence Homology
Sequence Homology, Amino Acid
Reproductive and Urinary Physiological Phenomena
Reproductive Physiological Phenomena
Maternal Age
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