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3. Craniofacial studies in chicken embryos confirm the pathogenicity of human FZD2 variants associated with Robinow syndrome. Tophkhane SS; Fu K; Verheyen EM; Richman JM Dis Model Mech; 2024 Jun; 17(6):. PubMed ID: 38967226 [TBL] [Abstract][Full Text] [Related]
4. Novel pathogenic genomic variants leading to autosomal dominant and recessive Robinow syndrome. Zhang C; Mazzeu JF; Eisfeldt J; Grochowski CM; White J; Akdemir ZC; Jhangiani SN; Muzny DM; Gibbs RA; Lindstrand A; Lupski JR; Sutton VR; Carvalho CMB Am J Med Genet A; 2021 Dec; 185(12):3593-3600. PubMed ID: 33048444 [TBL] [Abstract][Full Text] [Related]
5. Whole genome variant association across 100 dogs identifies a frame shift mutation in DISHEVELLED 2 which contributes to Robinow-like syndrome in Bulldogs and related screw tail dog breeds. Mansour TA; Lucot K; Konopelski SE; Dickinson PJ; Sturges BK; Vernau KL; Choi S; Stern JA; Thomasy SM; Döring S; Verstraete FJM; Johnson EG; York D; Rebhun RB; Ho HH; Brown CT; Bannasch DL PLoS Genet; 2018 Dec; 14(12):e1007850. PubMed ID: 30521570 [TBL] [Abstract][Full Text] [Related]
6. Nonsense mutations in FZD2 cause autosomal-dominant omodysplasia: Robinow syndrome-like phenotypes. Nagasaki K; Nishimura G; Kikuchi T; Nyuzuki H; Sasaki S; Ogawa Y; Saitoh A Am J Med Genet A; 2018 Mar; 176(3):739-742. PubMed ID: 29383834 [TBL] [Abstract][Full Text] [Related]
7. FZD2 regulates limb development by mediating β-catenin-dependent and -independent Wnt signaling pathways. Zhu X; Xu M; Leu NA; Morrisey EE; Millar SE Dis Model Mech; 2023 Mar; 16(3):. PubMed ID: 36867021 [TBL] [Abstract][Full Text] [Related]
8. DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome. White JJ; Mazzeu JF; Hoischen A; Bayram Y; Withers M; Gezdirici A; Kimonis V; Steehouwer M; Jhangiani SN; Muzny DM; Gibbs RA; ; van Bon BWM; Sutton VR; Lupski JR; Brunner HG; Carvalho CMB Am J Hum Genet; 2016 Mar; 98(3):553-561. PubMed ID: 26924530 [TBL] [Abstract][Full Text] [Related]
9. Mutations in DVL1 cause an osteosclerotic form of Robinow syndrome. Bunn KJ; Daniel P; Rösken HS; O'Neill AC; Cameron-Christie SR; Morgan T; Brunner HG; Lai A; Kunst HP; Markie DM; Robertson SP Am J Hum Genet; 2015 Apr; 96(4):623-30. PubMed ID: 25817014 [TBL] [Abstract][Full Text] [Related]
10. Autosomal dominant Robinow syndrome associated with a novel DVL3 splice mutation. Danyel M; Kortüm F; Dathe K; Kutsche K; Horn D Am J Med Genet A; 2018 Apr; 176(4):992-996. PubMed ID: 29575616 [TBL] [Abstract][Full Text] [Related]
11. DVL1 frameshift mutations clustering in the penultimate exon cause autosomal-dominant Robinow syndrome. White J; Mazzeu JF; Hoischen A; Jhangiani SN; Gambin T; Alcino MC; Penney S; Saraiva JM; Hove H; Skovby F; Kayserili H; Estrella E; Vulto-van Silfhout AT; Steehouwer M; Muzny DM; Sutton VR; Gibbs RA; ; Lupski JR; Brunner HG; van Bon BW; Carvalho CM Am J Hum Genet; 2015 Apr; 96(4):612-22. PubMed ID: 25817016 [TBL] [Abstract][Full Text] [Related]
12. Biallelic loss-of-function WNT5A mutations in an infant with severe and atypical manifestations of Robinow syndrome. Birgmeier J; Esplin ED; Jagadeesh KA; Guturu H; Wenger AM; Chaib H; Buckingham JA; Bejerano G; Bernstein JA Am J Med Genet A; 2018 Apr; 176(4):1030-1036. PubMed ID: 29575631 [TBL] [Abstract][Full Text] [Related]
13. Robinow syndrome skeletal phenotypes caused by the WNT5AC83S variant are due to dominant interference with chondrogenesis. Gignac SJ; Hosseini-Farahabadi S; Akazawa T; Schuck NJ; Fu K; Richman JM Hum Mol Genet; 2019 Jul; 28(14):2395-2414. PubMed ID: 31032853 [TBL] [Abstract][Full Text] [Related]
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15. Clinical and molecular characterization of four patients with Robinow syndrome from different families. Rai A; Patil SJ; Srivastava P; Gaurishankar K; Phadke SR Am J Med Genet A; 2021 Apr; 185(4):1105-1112. PubMed ID: 33496066 [TBL] [Abstract][Full Text] [Related]
16. A novel de-novo WNT5A mutation in a Chinese patient with Robinow syndrome. Xiong S; Chitayat D; Wei X; Zhu J; Lu W; Sun LM; Chopra M Clin Dysmorphol; 2016 Oct; 25(4):186-9. PubMed ID: 27092434 [No Abstract] [Full Text] [Related]
17. De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype. Roifman M; Marcelis CL; Paton T; Marshall C; Silver R; Lohr JL; Yntema HG; Venselaar H; Kayserili H; van Bon B; Seaward G; ; Brunner HG; Chitayat D Clin Genet; 2015; 87(1):34-41. PubMed ID: 24716670 [TBL] [Abstract][Full Text] [Related]
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