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MIM:613776 - CHROMOSOME 17p13.1 DELETION SYNDROME
Xenbase Genes:
Human Disease Resource: OMIM
MONDO:0013415 - chromosome 17p13.1 deletion syndrome |
DOID:0060402 - chromosome 17p13.1 deletion syndrome |
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MONDO:0013415 - chromosome 17p13.1 deletion syndrome |
DOID:0060402 - chromosome 17p13.1 deletion syndrome |