chromosome 17p11.2 deletion
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1
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Contents
1
Pathology
2
Genetics
3
More general terms
4
Additional terms
5
References
Pathology
defects in
RAI1
(& presumably
deletion
) are a cause of
Smith-Magenis syndrome
Genetics
locus
of
RAI1
gene
More general terms
gene/chromosomal deletion testing
Additional terms
human chromosome-17
References
↑
Loinc
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