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162220
NF3B
NEUROFIBROMATOSIS, FAMILIAL INTESTINAL
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Genetic Phenomena
Genetic Processes
Mutagenesis
Translocation, Genetic
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 12
Chromosomes, Human, 13-15
Chromosomes, Human, Pair 14
Genetic Variation
Mutation
Chromosome Aberrations
Translocation, Genetic
Database Center for Life Science
