Gurnett CA - Search Results

1

Comprehensive In Vivo Interrogation Reveals Phenotypic Impact of Human Enhancer Variants.

Kvon EZ, Zhu Y, Kelman G, Novak CS, Plajzer-Frick I, Kato M, Garvin TH, Pham Q, Harrington AN, Hunter RD, Godoy J, Meky EM, Akiyama JA, Afzal V, Tran S, Escande F, Gilbert-Dussardier B, Jean-Marçais N, Hudaiberdiev S, Ovcharenko I, Dobbs MB, Gurnett CA, Manouvrier-Hanu S, Petit F, Visel A, Dickel DE, Pennacchio LA. Kvon EZ, et al. Among authors: gurnett ca. Cell. 2020 Mar 19;180(6):1262-1271.e15. doi: 10.1016/j.cell.2020.02.031. Epub 2020 Mar 12. Cell. 2020. PMID: 32169219 Free PMC article.

2

Treatment of idiopathic clubfoot: an historical review.

Dobbs MB, Morcuende JA, Gurnett CA, Ponseti IV. Dobbs MB, et al. Among authors: gurnett ca. Iowa Orthop J. 2000;20:59-64. Iowa Orthop J. 2000. PMID: 10934626 Free PMC article.

3

Factors predictive of outcome after use of the Ponseti method for the treatment of idiopathic clubfeet.

Dobbs MB, Rudzki JR, Purcell DB, Walton T, Porter KR, Gurnett CA. Dobbs MB, et al. Among authors: gurnett ca. J Bone Joint Surg Am. 2004 Jan;86(1):22-7. doi: 10.2106/00004623-200401000-00005. J Bone Joint Surg Am. 2004. PMID: 14711941 Free article.

4

Flexor digitorum accessorius longus muscle is associated with familial idiopathic clubfoot.

Dobbs MB, Walton T, Gordon JE, Schoenecker PL, Gurnett CA. Dobbs MB, et al. Among authors: gurnett ca. J Pediatr Orthop. 2005 May-Jun;25(3):357-9. doi: 10.1097/01.bpo.0000152908.08422.95. J Pediatr Orthop. 2005. PMID: 15832155

5

Variable hand and foot abnormalities in family with congenital vertical talus and CDMP-1 gene mutation.

Dobbs MB, Gurnett CA, Robarge J, Gordon JE, Morcuende JA, Bowcock AM. Dobbs MB, et al. Among authors: gurnett ca. J Orthop Res. 2005 Nov;23(6):1490-4. doi: 10.1016/j.orthres.2005.04.011.1100230636. Epub 2005 Jul 11. J Orthop Res. 2005. PMID: 16005596 Free article.

6

Evidence for an additional locus for split hand/foot malformation in chromosome region 8q21.11-q22.3.

Gurnett CA, Dobbs MB, Nordsieck EJ, Keppel C, Goldfarb CA, Morcuende JA, Bowcock AM. Gurnett CA, et al. Am J Med Genet A. 2006 Aug 15;140(16):1744-8. doi: 10.1002/ajmg.a.31375. Am J Med Genet A. 2006. PMID: 16838310

7

Two novel point mutations in the long-range SHH enhancer in three families with triphalangeal thumb and preaxial polydactyly.

Gurnett CA, Bowcock AM, Dietz FR, Morcuende JA, Murray JC, Dobbs MB. Gurnett CA, et al. Am J Med Genet A. 2007 Jan 1;143A(1):27-32. doi: 10.1002/ajmg.a.31563. Am J Med Genet A. 2007. PMID: 17152067

8

Absence of HOXD10 mutations in idiopathic clubfoot and sporadic vertical talus.

Gurnett CA, Keppel C, Bick J, Bowcock AM, Dobbs MB. Gurnett CA, et al. Clin Orthop Relat Res. 2007 Sep;462:27-31. doi: 10.1097/BLO.0b013e31805d8649. Clin Orthop Relat Res. 2007. PMID: 17417092

9

Case report: Congenital knee dislocation in a patient with larsen syndrome and a novel filamin B mutation.

Dobbs MB, Boehm S, Grange DK, Gurnett CA. Dobbs MB, et al. Among authors: gurnett ca. Clin Orthop Relat Res. 2008 Jun;466(6):1503-9. doi: 10.1007/s11999-008-0196-5. Epub 2008 Mar 6. Clin Orthop Relat Res. 2008. PMID: 18322662 Free PMC article.

10

Impact of congenital talipes equinovarus etiology on treatment outcomes.

Gurnett CA, Boehm S, Connolly A, Reimschisel T, Dobbs MB. Gurnett CA, et al. Dev Med Child Neurol. 2008 Jul;50(7):498-502. doi: 10.1111/j.1469-8749.2008.03016.x. Dev Med Child Neurol. 2008. PMID: 18611198 Free article. Clinical Trial.

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