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Items: 4

1.
Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE
C Nava, F Lamari, D Héron, C Mignot, A Rastetter, B Keren, D Cohen, A Faudet, D Bouteiller, M Gilleron, A Jacquette, S Whalen, A Afenjar, D Périsse, C Laurent, C Dupuits, C Gautier, M Gérard, G Huguet, S Caillet, B Leheup, M Leboyer, C Gillberg, R Delorme, T Bourgeron, A Brice, C Depienne
Transl Psychiatry. 2012 Oct; 2(10): e179. Published online 2012 Oct 23. doi: 10.1038/tp.2012.102
PMCID:
PMC3565810
ArticlePDF–1.1M
2.
The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)
Genome Res. 2004 Oct; 14(10b): 2121–2127. doi: 10.1101/gr.2596504
Correction in:
Genome Res. 2006 Jun; 16(6): 804.
PMCID:
PMC528928
ArticlePDF–140K
3.
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences
Mammalian Gene Collection (MGC) Program Team
Proc Natl Acad Sci U S A. 2002 Dec 24; 99(26): 16899–16903. Published online 2002 Dec 11. doi: 10.1073/pnas.242603899
PMCID:
PMC139241
ArticlePDF–118K
4.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas
Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042
PMCID:
PMC3178059
ArticlePDF–1.0M

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