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Hypercholesterolemia in children with Smith-Magenis syndrome: del (17) (p11.2p11.2).
Genet Med. 2002 May-Jun;4(3):118-25. doi: 10.1097/00125817-200205000-00004.
Genet Med. 2002.
PMID: 12180145
Free article.
Refinement of the Smith-Magenis syndrome critical region to approximately 950kb and assessment of 17p11.2 deletions. Are all deletions created equally?
Vlangos CN, Yim DK, Elsea SH.
Vlangos CN, et al.
Mol Genet Metab. 2003 Jun;79(2):134-41. doi: 10.1016/s1096-7192(03)00048-9.
Mol Genet Metab. 2003.
PMID: 12809645
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