Rogers RC - 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: rogers rc. 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

Cytogenetic, biochemical, and molecular analyses of a 22q13 deletion.

Phelan MC, Thomas GR, Saul RA, Rogers RC, Taylor HA, Wenger DA, McDermid HE. Phelan MC, et al. Among authors: rogers rc. Am J Med Genet. 1992 Jul 15;43(5):872-6. doi: 10.1002/ajmg.1320430524. Am J Med Genet. 1992. PMID: 1353666

3

Fragile-X syndrome.

Simensen RJ, Rogers RC. Simensen RJ, et al. Among authors: rogers rc. Am Fam Physician. 1989 May;39(5):185-93. Am Fam Physician. 1989. PMID: 2655406 Review.

4

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

5

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

6

Fragile X syndrome: a common etiology of mental retardation.

Rogers RC, Simensen RJ. Rogers RC, et al. Am J Ment Defic. 1987 Mar;91(5):445-9. Am J Ment Defic. 1987. PMID: 3565490

7

Albright hereditary osteodystrophy and del(2) (q37.3) in four unrelated individuals.

Phelan MC, Rogers RC, Clarkson KB, Bowyer FP, Levine MA, Estabrooks LL, Severson MC, Dobyns WB. Phelan MC, et al. Among authors: rogers rc. Am J Med Genet. 1995 Jul 31;58(1):1-7. doi: 10.1002/ajmg.1320580102. Am J Med Genet. 1995. PMID: 7573148

8

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

9

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

10

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

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