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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2009 | 1 |
2010 | 2 |
2011 | 1 |
2024 | 0 |
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Genome-wide identification of mouse congenital heart disease loci.
Hum Mol Genet. 2010 Aug 15;19(16):3105-13. doi: 10.1093/hmg/ddq211. Epub 2010 May 28.
Hum Mol Genet. 2010.
PMID: 20511334
Free PMC article.
Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome.
Cui C, Chatterjee B, Francis D, Yu Q, SanAgustin JT, Francis R, Tansey T, Henry C, Wang B, Lemley B, Pazour GJ, Lo CW.
Cui C, et al.
Dis Model Mech. 2011 Jan;4(1):43-56. doi: 10.1242/dmm.006262. Epub 2010 Nov 2.
Dis Model Mech. 2011.
PMID: 21045211
Free PMC article.
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A mouse model for Meckel syndrome reveals Mks1 is required for ciliogenesis and Hedgehog signaling.
Weatherbee SD, Niswander LA, Anderson KV.
Weatherbee SD, et al.
Hum Mol Genet. 2009 Dec 1;18(23):4565-75. doi: 10.1093/hmg/ddp422. Epub 2009 Sep 22.
Hum Mol Genet. 2009.
PMID: 19776033
Free PMC article.
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