HIGHLIGHTS
- who: Wenjuan Tang from the (UNIVERSITY) have published the research: Prenatal diagnosis and genetic counseling of a paternally inherited chromosome 15q11.2 microdeletion in a Chinese family, in the Journal: (JOURNAL)
- future: Due to incomplete penetrance and variable expressivity not all individuals with this microdeletion will present with these typical clinical manifestations and microdeletions or duplications in 15q11.2 are present in 0.5% to 1.0% of the population so more research is needed on causation and genetic counseling.
SUMMARY
Recurrent microdeletions and duplications in the genomic region 15q11.2 . . .
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