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Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype.
J Med Genet. 2002 Aug;39(8):594-6. doi: 10.1136/jmg.39.8.594.
J Med Genet. 2002.
PMID: 12161602
Free PMC article.
No abstract available.
Profound obesity associated with a balanced translocation that disrupts the SIM1 gene.
Holder JL Jr, Butte NF, Zinn AR.
Holder JL Jr, et al.
Hum Mol Genet. 2000 Jan 1;9(1):101-8. doi: 10.1093/hmg/9.1.101.
Hum Mol Genet. 2000.
PMID: 10587584
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