Rogers RC - Search Results

1

FG syndrome, an X-linked multiple congenital anomaly syndrome: the clinical phenotype and an algorithm for diagnostic testing.

Clark RD, Graham JM Jr, Friez MJ, Hoo JJ, Jones KL, McKeown C, Moeschler JB, Raymond FL, Rogers RC, Schwartz CE, Battaglia A, Lyons MJ, Stevenson RE. Clark RD, et al. Among authors: rogers rc. Genet Med. 2009 Nov;11(11):769-75. doi: 10.1097/GIM.0b013e3181bd3d90. Genet Med. 2009. PMID: 19938245 Free PMC article.

2

Fragile X syndrome: growth, development, and intellectual function.

Prouty LA, Rogers RC, Stevenson RE, Dean JH, Palmer KK, Simensen RJ, Coston GN, Schwartz CE. Prouty LA, et al. Among authors: rogers rc. Am J Med Genet. 1988 May-Jun;30(1-2):123-42. doi: 10.1002/ajmg.1320300111. Am J Med Genet. 1988. PMID: 3177438

3

Fragile X syndrome: incidence, clinical and cytogenetic findings in the black and white populations of South Carolina.

Schwartz CE, Phelan MC, Pulliam LH, Wilkes G, Vanner LV, Albiez KL, Potts WA, Rogers RC, Schroer RJ, Saul RA, et al. Schwartz CE, et al. Among authors: rogers rc. Am J Med Genet. 1988 May-Jun;30(1-2):641-54. doi: 10.1002/ajmg.1320300165. Am J Med Genet. 1988. PMID: 3177476

4

Brachmann-de Lange syndrome: diagnostic difficulties posed by the mild phenotype.

Saul RA, Rogers RC, Phelan MC, Stevenson RE. Saul RA, et al. Among authors: rogers rc. Am J Med Genet. 1993 Nov 15;47(7):999-1002. doi: 10.1002/ajmg.1320470712. Am J Med Genet. 1993. PMID: 8291544

5

Two patients with duplication of 17p11.2: the reciprocal of the Smith-Magenis syndrome deletion?

Brown A, Phelan MC, Patil S, Crawford E, Rogers RC, Schwartz C. Brown A, et al. Among authors: rogers rc. Am J Med Genet. 1996 May 17;63(2):373-7. doi: 10.1002/(SICI)1096-8628(19960517)63:2<373::AID-AJMG9>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8725788

6

Clinical and behavioral characteristics in FG syndrome.

Graham JM Jr, Superneau D, Rogers RC, Corning K, Schwartz CE, Dykens EM. Graham JM Jr, et al. Among authors: rogers rc. Am J Med Genet. 1999 Aug 27;85(5):470-5. Am J Med Genet. 1999. PMID: 10405444

7

Germline mosaicism in X-linked myotubular myopathy.

Häne BG, Rogers RC, Schwartz CE. Häne BG, et al. Among authors: rogers rc. Clin Genet. 1999 Jul;56(1):77-81. doi: 10.1034/j.1399-0004.1999.560111.x. Clin Genet. 1999. PMID: 10466421

8

P63 mutations are not a major cause of non-syndromic split hand/foot malformation.

de Mollerat XJ, Everman DB, Morgan CT, Clarkson KB, Rogers RC, Colby RS, Aylsworth AS, Graham JM Jr, Stevenson RE, Schwartz CE. de Mollerat XJ, et al. Among authors: rogers rc. J Med Genet. 2003 Jan;40(1):55-61. doi: 10.1136/jmg.40.1.55. J Med Genet. 2003. PMID: 12525544 Free PMC article. No abstract available.

9

Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene.

Schwartz CE, May MM, Carpenter NJ, Rogers RC, Martin J, Bialer MG, Ward J, Sanabria J, Marsa S, Lewis JA, Echeverri R, Lubs HA, Voeller K, Simensen RJ, Stevenson RE. Schwartz CE, et al. Among authors: rogers rc. Am J Hum Genet. 2005 Jul;77(1):41-53. doi: 10.1086/431313. Epub 2005 May 11. Am J Hum Genet. 2005. PMID: 15889350 Free PMC article.

10

X-linked MCT8 gene mutations: characterization of the pediatric neurologic phenotype.

Holden KR, Zuñiga OF, May MM, Su H, Molinero MR, Rogers RC, Schwartz CE. Holden KR, et al. Among authors: rogers rc. J Child Neurol. 2005 Oct;20(10):852-7. doi: 10.1177/08830738050200101601. J Child Neurol. 2005. PMID: 16417886

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