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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 1
2002 1
2003 1
2004 2
2005 1
2006 6
2007 3
2009 3
2010 3
2011 2
2012 1
2013 2
2014 1
2015 1
2017 3
2018 2
2019 3
2020 1
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Article type
Publication date

Cited In for PMID: 10923031

31 results
Results by year
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Page 1
Mutations in holoprosencephaly.
Wallis D, Muenke M. Wallis D, et al. Hum Mutat. 2000;16(2):99-108. doi: 10.1002/1098-1004(200008)16:2<99::AID-HUMU2>3.0.CO;2-0. Hum Mutat. 2000. PMID: 10923031 Review.
Schilbach-Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene.
Prontera P, Rogaia D, Sallicandro E, Mencarelli A, Imperatore V, Squeo GM, Merla G, Elisei S, Moretti-Ferreira D, Esposito S, Stangoni G. Prontera P, et al. Eur J Hum Genet. 2019 Aug;27(8):1260-1266. doi: 10.1038/s41431-019-0385-6. Epub 2019 Apr 1. Eur J Hum Genet. 2019. PMID: 30936464
The hedgehog pathway and ocular developmental anomalies.
Cavodeassi F, Creuzet S, Etchevers HC. Cavodeassi F, et al. Hum Genet. 2019 Sep;138(8-9):917-936. doi: 10.1007/s00439-018-1918-8. Epub 2018 Aug 2. Hum Genet. 2019. PMID: 30073412 Free PMC article. Review.
Ethanol itself is a holoprosencephaly-inducing teratogen.
Hong M, Krauss RS. Hong M, et al. PLoS One. 2017 Apr 25;12(4):e0176440. doi: 10.1371/journal.pone.0176440. eCollection 2017. PLoS One. 2017. PMID: 28441416 Free PMC article.
Developmental disorders of the dentition: an update.
Klein OD, Oberoi S, Huysseune A, Hovorakova M, Peterka M, Peterkova R. Klein OD, et al. Am J Med Genet C Semin Med Genet. 2013 Nov;163C(4):318-32. doi: 10.1002/ajmg.c.31382. Epub 2013 Oct 4. Am J Med Genet C Semin Med Genet. 2013. PMID: 24124058 Free PMC article. Review.
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