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Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function.
Proc Natl Acad Sci U S A. 2004 Aug 10;101(32):11689-94. doi: 10.1073/pnas.0401194101. Epub 2004 Jul 23.
Proc Natl Acad Sci U S A. 2004.
PMID: 15273283
Free PMC article.
Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2.
Strauss KA, Puffenberger EG, Huentelman MJ, Gottlieb S, Dobrin SE, Parod JM, Stephan DA, Morton DH.
Strauss KA, et al. Among authors: parod jm.
N Engl J Med. 2006 Mar 30;354(13):1370-7. doi: 10.1056/NEJMoa052773.
N Engl J Med. 2006.
PMID: 16571880
Free article.
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Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA.
Ma DQ, et al. Among authors: parod j.
Mol Psychiatry. 2007 Apr;12(4):376-84. doi: 10.1038/sj.mp.4001927. Epub 2006 Dec 19.
Mol Psychiatry. 2007.
PMID: 17179998
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