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Results by year

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

Year Number of Results
1969 1
1986 1
1992 1
1995 1
1997 1
1998 2
2000 4
2001 2
2002 2
2003 3
2005 1
2006 1
2007 1
2008 2
2009 1
2011 1
2015 1
2016 1
2017 2
2018 1
2023 0

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PubMed (Bookshelf cited) for id: 1770070

28 results

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Page 1
WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome.
White JJ, Mazzeu JF, Coban-Akdemir Z, Bayram Y, Bahrambeigi V, Hoischen A, van Bon BWM, Gezdirici A, Gulec EY, Ramond F, Touraine R, Thevenon J, Shinawi M, Beaver E, Heeley J, Hoover-Fong J, Durmaz CD, Karabulut HG, Marzioglu-Ozdemir E, Cayir A, Duz MB, Seven M, Price S, Ferreira BM, Vianna-Morgante AM, Ellard S, Parrish A, Stals K, Flores-Daboub J, Jhangiani SN, Gibbs RA; Baylor-Hopkins Center for Mendelian Genomics; Brunner HG, Sutton VR, Lupski JR, Carvalho CMB. White JJ, et al. Am J Hum Genet. 2018 Jan 4;102(1):27-43. doi: 10.1016/j.ajhg.2017.10.002. Epub 2017 Dec 21. Am J Hum Genet. 2018. PMID: 29276006 Free PMC article.
ROR-Family Receptor Tyrosine Kinases.
Stricker S, Rauschenberger V, Schambony A. Stricker S, et al. Curr Top Dev Biol. 2017;123:105-142. doi: 10.1016/bs.ctdb.2016.09.003. Epub 2016 Oct 31. Curr Top Dev Biol. 2017. PMID: 28236965 Review.
Craniofacial and intraoral phenotype of Robinow syndrome forms.
Beiraghi S, Leon-Salazar V, Larson BE, John MT, Cunningham ML, Petryk A, Lohr JL. Beiraghi S, et al. Clin Genet. 2011 Jul;80(1):15-24. doi: 10.1111/j.1399-0004.2011.01683.x. Epub 2011 May 16. Clin Genet. 2011. PMID: 21496006
28 results