Gene Symbol
Gene Name
Aliases
Previous_Symbol
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MeSH term
Frequency
Condition_Probility
Animals
Humans
Mutation
Research Support, Non-U.S. Gov't
Phenotype
Base Sequence
Chromosome Disorders
*Chromosomes, Human, Pair 17
Female
High Mobility Group Proteins/*genetics
Infant, Newborn
Molecular Sequence Data
Osteochondrodysplasias/*genetics
Transcription Factors/*genetics
*Translocation, Genetic
Amino Acid Sequence
Chromosome Mapping
Male
*Sex Reversal, Gonadal
Translocation, Genetic
Genetic Markers
In Situ Hybridization, Fluorescence
Adult
Gonadal Dysgenesis/*genetics
Polymerase Chain Reaction