Clinical report: inherited deletion of chromosome 12q21.31q21.32 associated with a distinct phenotype and intellectual disability.

Akilapa, Rhoda S

Clinical report: inherited deletion of chromosome 12q21.31q21.32 associated with a distinct phenotype and intellectual disability. [electronic resource] - Clinical dysmorphology Oct 2015 - 151-5 p. digital

Publication Type: Case Reports; Journal Article

1473-5717

10.1097/MCD.0000000000000096 doi


Adult
Child
Chromosome Deletion
Chromosomes, Human, Pair 12
DNA Copy Number Variations
Genetic Association Studies
Humans
Intellectual Disability--genetics
Male
Sequence Deletion