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Query OMIM entry list
193520
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WATSON SYNDROME
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Molecular Conformation
Protein Conformation
Protein Structure, Tertiary
Genetic Phenomena
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 16-18
Chromosomes, Human, Pair 17
Genetic Code
Codon
Genome
Genome Components
DNA, Intergenic
Introns
Genes
Alleles
Gene Components
Codon
Exons
Introns
Genes, Neoplasm
Genes, Tumor Suppressor
Genes, Neurofibromatosis 1
Genes, Recessive
Genes, Tumor Suppressor
Genes, Neurofibromatosis 1
Multigene Family
Genetic Variation
Mutation
Mutation, Missense
Point Mutation
Polymorphism, Genetic
Polymorphism, Restriction Fragment Length
Polymorphism, Single-Stranded Conformational
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Database Center for Life Science
