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Enlarged Sylvian fissures in infants with interstitial deletion of chromosome 22q11.
Am J Med Genet. 1997 Sep 19;74(5):538-43.
Am J Med Genet. 1997.
PMID: 9342208
Arthrogryposis due to infantile neuronal degeneration associated with deletion of the SMNT gene.
Bingham PM, Shen N, Rennert H, Rorke LB, Black AW, Marin-Padilla MM, Nordgren RE.
Bingham PM, et al.
Neurology. 1997 Sep;49(3):848-51. doi: 10.1212/wnl.49.3.848.
Neurology. 1997.
PMID: 9305352
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