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Query OMIM entry list
141750
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ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, DELETION-TYPE
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Chemical Phenomena
Biochemical Phenomena
Biochemical Processes
DNA Repair
Nucleic Acid Hybridization
Molecular Structure
Amino Acid Sequence
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Structure-Activity Relationship
Chemical Processes
Biochemical Processes
DNA Repair
Nucleic Acid Hybridization
Genetic Phenomena
Genetic Processes
DNA Repair
Gene Rearrangement
Mutagenesis
Sequence Deletion
Chromosome Deletion
Gene Deletion
Translocation, Genetic
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Chromosome Structures
Telomere
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 3
Chromosomes, Human, 13-15
Chromosomes, Human, Pair 13
Chromosomes, Human, 16-18
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 18
Chromosomes, Human, 21-22 and Y
Chromosomes, Human, Pair 22
Genome
Genome Components
Genes
Multigene Family
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Translocation, Genetic
Point Mutation
Sequence Deletion
Chromosome Deletion
Gene Deletion
Polymorphism, Genetic
Polymorphism, Restriction Fragment Length
Genotype
Heterozygote
Genetic Linkage
Lod Score
Phenotype
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Physiological Phenomena
Organ Specificity
Pharmacological Phenomena
Structure-Activity Relationship
Database Center for Life Science
