Genetics and Chromosome 16q22 deletion syndrome

Associated cytogenetic location

  • Location: 16q22

Source: GTR (NCBI/NIH)1

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Inheritance of Chromosome 16q22 deletion syndrome

Genetic and familial features of the condition may include:2 Genetics of Chromosome 16q22 Deletion Syndrome:

  • Sporadic


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References

  1. Source: GTR (NCBI/NIH): ncbi.nlm.nih.gov/ gtr/ conditions/ C3281152/ 
  2. Source: Human Phenotype Ontology

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