PubMed (Bookshelf cited) for id: 1770070

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

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.

2

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.

3

Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel ROR2 gene mutations.

Aglan M, Amr K, Ismail S, Ashour A, Otaify GA, Mehrez MA, Aboul-Ezz EH, El-Ruby M, Mazen I, Abdel-Hamid MS, Temtamy SA. Aglan M, et al. Am J Med Genet A. 2015 Dec;167A(12):3054-61. doi: 10.1002/ajmg.a.37287. Epub 2015 Aug 18. Am J Med Genet A. 2015. PMID: 26284319

4

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

5

A gradient of ROR2 protein stability and membrane localization confers brachydactyly type B or Robinow syndrome phenotypes.

Schwarzer W, Witte F, Rajab A, Mundlos S, Stricker S. Schwarzer W, et al. Hum Mol Genet. 2009 Nov 1;18(21):4013-21. doi: 10.1093/hmg/ddp345. Epub 2009 Jul 29. Hum Mol Genet. 2009. PMID: 19640924

6

Robinow syndrome: phenotypic variability in a family with a novel intragenic ROR2 mutation.

Brunetti-Pierri N, Del Gaudio D, Peters H, Justino H, Ott CE, Mundlos S, Bacino CA. Brunetti-Pierri N, et al. Am J Med Genet A. 2008 Nov 1;146A(21):2804-9. doi: 10.1002/ajmg.a.32530. Am J Med Genet A. 2008. PMID: 18831060

7

Autosomal recessive Robinow syndrome: a case report.

Grothe R, Anderson-Cermin C, Beiraghi S. Grothe R, et al. J Dent Child (Chic). 2008 Jan-Apr;75(1):48-54. J Dent Child (Chic). 2008. PMID: 18505648

8

Clinical characterization of autosomal dominant and recessive variants of Robinow syndrome.

Mazzeu JF, Pardono E, Vianna-Morgante AM, Richieri-Costa A, Ae Kim C, Brunoni D, Martelli L, de Andrade CE, Colin G, Otto PA. Mazzeu JF, et al. Am J Med Genet A. 2007 Feb 15;143(4):320-5. doi: 10.1002/ajmg.a.31592. Am J Med Genet A. 2007. PMID: 17256787

9

Prenatal and postnatal findings in a case with the autosomal recessive type of Robinow syndrome.

Guven MA, Batukan C, Ceylaner S, Uzel M, Ozbek A, Demirpolat G. Guven MA, et al. Fetal Diagn Ther. 2006;21(4):386-9. doi: 10.1159/000092471. Fetal Diagn Ther. 2006. PMID: 16757917

10

Clinical and molecular characterization of two adults with autosomal recessive Robinow syndrome.

Tufan F, Cefle K, Türkmen S, Türkmen A, Zorba U, Dursun M, Oztürk S, Palandüz S, Ecder T, Mundlos S, Horn D. Tufan F, et al. Am J Med Genet A. 2005 Jul 15;136(2):185-9. doi: 10.1002/ajmg.a.30785. Am J Med Genet A. 2005. PMID: 15952209

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