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Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability.
Mol Cytogenet. 2014 Dec 31;7(1):97. doi: 10.1186/s13039-014-0097-0. eCollection 2014.
Mol Cytogenet. 2014.
PMID: 25606055
Free PMC article.
[MR scanning of cerebrum in the investigation of delayed development in children. Syntelencephaly--is it really so rare?].
Schultz-Pedersen S, Balslev T, Christensen T.
Schultz-Pedersen S, et al.
Ugeskr Laeger. 2002 Sep 2;164(36):4188-90.
Ugeskr Laeger. 2002.
PMID: 12362834
Danish.
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Evidence of decreased risk of cancer in individuals with fragile X.
Schultz-Pedersen S, Hasle H, Olsen JH, Friedrich U.
Schultz-Pedersen S, et al.
Am J Med Genet. 2001 Oct 15;103(3):226-30.
Am J Med Genet. 2001.
PMID: 11745995
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