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128 results

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Page 1
Lack of evidence of WNT3A as a candidate gene for congenital vertebral malformations.
Ghebranious N, Raggio CL, Blank RD, McPherson E, Burmester JK, Ivacic L, Rasmussen K, Kislow J, Glurich I, Jacobsen FS, Faciszewski T, Pauli RM, Boachie-Adjei O, Giampietro PF. Ghebranious N, et al. Among authors: blank rd. Scoliosis. 2007 Sep 23;2:13. doi: 10.1186/1748-7161-2-13. Scoliosis. 2007. PMID: 17888180 Free PMC article.
Evaluation of SLC35A3 as a candidate gene for human vertebral malformations.
Ghebranious N, Burmester JK, Glurich I, McPherson E, Ivacic L, Kislow J, Rasmussen K, Kumar V, Raggio CL, Blank RD, Jacobsen FS, Faciszewski T, Womack J, Giampietro PF. Ghebranious N, et al. Among authors: blank rd. Am J Med Genet A. 2006 Jun 15;140(12):1346-8. doi: 10.1002/ajmg.a.31307. Am J Med Genet A. 2006. PMID: 16691598 No abstract available.
DLL3 as a candidate gene for vertebral malformations.
Giampietro PF, Raggio CL, Reynolds C, Ghebranious N, Burmester JK, Glurich I, Rasmussen K, McPherson E, Pauli RM, Shukla SK, Merchant S, Jacobsen FS, Faciszewski T, Blank RD. Giampietro PF, et al. Among authors: blank rd. Am J Med Genet A. 2006 Nov 15;140(22):2447-53. doi: 10.1002/ajmg.a.31509. Am J Med Genet A. 2006. PMID: 17041936
A missense T (Brachyury) mutation contributes to vertebral malformations.
Ghebranious N, Blank RD, Raggio CL, Staubli J, McPherson E, Ivacic L, Rasmussen K, Jacobsen FS, Faciszewski T, Burmester JK, Pauli RM, Boachie-Adjei O, Glurich I, Giampietro PF. Ghebranious N, et al. Among authors: blank rd. J Bone Miner Res. 2008 Oct;23(10):1576-83. doi: 10.1359/jbmr.080503. J Bone Miner Res. 2008. PMID: 18466071 Free article.
Congenital and idiopathic scoliosis: clinical and genetic aspects.
Giampietro PF, Blank RD, Raggio CL, Merchant S, Jacobsen FS, Faciszewski T, Shukla SK, Greenlee AR, Reynolds C, Schowalter DB. Giampietro PF, et al. Among authors: blank rd. Clin Med Res. 2003 Apr;1(2):125-36. doi: 10.3121/cmr.1.2.125. Clin Med Res. 2003. PMID: 15931299 Free PMC article. Review.
Heterozygous mutations in the T (brachyury) gene.
Giampietro PF, Raggio CL, Blank RD. Giampietro PF, et al. Among authors: blank rd. J Med Genet. 2014 May;51(5):354. doi: 10.1136/jmedgenet-2014-102308. Epub 2014 Feb 20. J Med Genet. 2014. PMID: 24556085 No abstract available.
An analysis of PAX1 in the development of vertebral malformations.
Giampietro PF, Raggio CL, Reynolds CE, Shukla SK, McPherson E, Ghebranious N, Jacobsen FS, Kumar V, Faciszewski T, Pauli RM, Rasmussen K, Burmester JK, Zaleski C, Merchant S, David D, Weber JL, Glurich I, Blank RD. Giampietro PF, et al. Among authors: blank rd. Clin Genet. 2005 Nov;68(5):448-53. doi: 10.1111/j.1399-0004.2005.00520.x. Clin Genet. 2005. PMID: 16207213
KIAA1217: A novel candidate gene associated with isolated and syndromic vertebral malformations.
Al Dhaheri N, Wu N, Zhao S, Wu Z, Blank RD, Zhang J, Raggio C, Halanski M, Shen J, Noonan K, Qiu G, Nemeth B, Sund S, Dunwoodie SL, Chapman G, Glurich I, Steiner RD, Wohler E, Martin R, Sobreira NL, Giampietro PF. Al Dhaheri N, et al. Among authors: blank rd. Am J Med Genet A. 2020 Jul;182(7):1664-1672. doi: 10.1002/ajmg.a.61607. Epub 2020 May 5. Am J Med Genet A. 2020. PMID: 32369272 Free PMC article.
128 results