Hunter AG - Search Results

1

Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndrome.

Lyons MJ, Graham JM Jr, Neri G, Hunter AG, Clark RD, Rogers RC, Moscarda M, Boccuto L, Simensen R, Dodd J, Robertson S, DuPont BR, Friez MJ, Schwartz CE, Stevenson RE. Lyons MJ, et al. Among authors: hunter ag. J Med Genet. 2009 Jan;46(1):9-13. doi: 10.1136/jmg.2008.060509. Epub 2008 Sep 19. J Med Genet. 2009. PMID: 18805826

2

The Hunter-McAlpine syndrome results from duplication 5q35-qter.

Hunter AG, Dupont B, McLaughlin M, Hinton L, Baker E, Adès L, Haan E, Schwartz CE. Hunter AG, et al. Clin Genet. 2005 Jan;67(1):53-60. doi: 10.1111/j.1399-0004.2005.00378.x. Clin Genet. 2005. PMID: 15617549

3

Further delineation of Kabuki syndrome in 48 well-defined new individuals.

Armstrong L, Abd El Moneim A, Aleck K, Aughton DJ, Baumann C, Braddock SR, Gillessen-Kaesbach G, Graham JM Jr, Grebe TA, Gripp KW, Hall BD, Hennekam R, Hunter A, Keppler-Noreuil K, Lacombe D, Lin AE, Ming JE, Kokitsu-Nakata NM, Nikkel SM, Philip N, Raas-Rothschild A, Sommer A, Verloes A, Walter C, Wieczorek D, Williams MS, Zackai E, Allanson JE. Armstrong L, et al. Am J Med Genet A. 2005 Jan 30;132A(3):265-72. doi: 10.1002/ajmg.a.30340. Am J Med Genet A. 2005. PMID: 15690370

4

Gastroschisis: clinical presentation and associations.

Hunter AG, Stevenson RE. Hunter AG, et al. Am J Med Genet C Semin Med Genet. 2008 Aug 15;148C(3):219-30. doi: 10.1002/ajmg.c.30178. Am J Med Genet C Semin Med Genet. 2008. PMID: 18655099

5

Escape of the yolk sac: a hypothesis to explain the embryogenesis of gastroschisis.

Stevenson RE, Rogers RC, Chandler JC, Gauderer MW, Hunter AG. Stevenson RE, et al. Among authors: hunter ag. Clin Genet. 2009 Apr;75(4):326-33. doi: 10.1111/j.1399-0004.2008.01142.x. Clin Genet. 2009. PMID: 19419415

6

Detailed assessment of the ear in Cornelia de Lange syndrome: comparison with a control sample using the new dysmorphology guidelines.

Hunter AG, Collins JS, Deardorff MA, Krantz ID. Hunter AG, et al. Am J Med Genet A. 2009 Oct;149A(10):2181-92. doi: 10.1002/ajmg.a.33073. Am J Med Genet A. 2009. PMID: 19764039 Free PMC article.

7

Limb-body wall defect. Is there a defensible hypothesis and can it explain all the associated anomalies?

Hunter AG, Seaver LH, Stevenson RE. Hunter AG, et al. Am J Med Genet A. 2011 Sep;155A(9):2045-59. doi: 10.1002/ajmg.a.34161. Epub 2011 Aug 3. Am J Med Genet A. 2011. PMID: 21815262 Review.

8

Considering the Embryopathogenesis of VACTERL Association.

Stevenson RE, Hunter AG. Stevenson RE, et al. Among authors: hunter ag. Mol Syndromol. 2013 Feb;4(1-2):7-15. doi: 10.1159/000346192. Mol Syndromol. 2013. PMID: 23653571 Free PMC article.

9

The intellectual disabilities evaluation and advice system (IDEAS): outcome of the first 55 cases.

Hunter AG, Graham JM Jr, Neri G, Rogers RC, Stevenson RE, Turner G, Friez MJ. Hunter AG, et al. Am J Med Genet A. 2014 May;164A(5):1102-17. doi: 10.1002/ajmg.a.36456. Epub 2014 Mar 24. Am J Med Genet A. 2014. PMID: 24665081

10

Personal journeys to and in human genetics and dysmorphology.

Schwartz CE, Aylsworth AS, Allanson J, Battaglia A, Carey JC, Curry CJ, Davies KE, Eichler EE, Graham JM Jr, Hall B, Hall JG, Holmes LB, Hoyme HE, Hunter A, Innis J, Johnson J, Keppler-Noreuil KM, Leroy JG, Moore C, Nelson DL, Neri G, Opitz JM, Picketts D, Raymond FL, Shalev SA, Stevenson RE, Stumpel CTRM, Sutherland G, Viskochil DH, Weaver DD, Zackai EH. Schwartz CE, et al. Am J Med Genet A. 2024 Jun;194(6):e63514. doi: 10.1002/ajmg.a.63514. Epub 2024 Feb 8. Am J Med Genet A. 2024. PMID: 38329159

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