Schwartz CE - 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: schwartz ce. 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

Direct analysis of the FMR-1 gene provides an explanation for an exceptional case of a fragile X negative, mentally retarded male in a fragile X family.

Tarleton J, Wong S, Schwartz C. Tarleton J, et al. J Med Genet. 1992 Dec;29(12):919-20. doi: 10.1136/jmg.29.12.919. J Med Genet. 1992. PMID: 1336058 Free PMC article. No abstract available.

3

Difficult diagnosis of the fragile X syndrome made possible by direct detection of DNA mutations.

Tarleton J, Wong S, Heitz D, Schwartz C. Tarleton J, et al. J Med Genet. 1992 Oct;29(10):726-9. doi: 10.1136/jmg.29.10.726. J Med Genet. 1992. PMID: 1359145 Free PMC article.

4

Longitudinal changes in IQ among fragile X males: clinical evidence of more than one mutation?

Fisch GS, Shapiro LR, Simensen R, Schwartz CE, Fryns JP, Borghgraef M, Curfs LM, Howard-Peebles PN, Arinami T, Mavrou A. Fisch GS, et al. Among authors: schwartz ce. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):28-34. doi: 10.1002/ajmg.1320430105. Am J Med Genet. 1992. PMID: 1605202

5

MRX8: an X-linked mental retardation condition with linkage to Xq21.

Schwartz CE, May M, Huang T, Ledbetter D, Anderson G, Barker DF, Lubs HA, Arena F, Stevenson RE. Schwartz CE, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):467-74. doi: 10.1002/ajmg.1320430170. Am J Med Genet. 1992. PMID: 1605227

6

Spastic paraplegia with iron deposits in the basal ganglia: a new X-linked mental retardation syndrome.

Arena JF, Schwartz C, Stevenson R, Lawrence L, Carpenter A, Duara R, Ledbetter D, Huang T, Lehner T, Ott J, et al. Arena JF, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):479-90. doi: 10.1002/ajmg.1320430172. Am J Med Genet. 1992. PMID: 1605230

7

Allan-Herndon-Dudley syndrome: clinical and linkage studies on a second family.

Bialer MG, Lawrence L, Stevenson RE, Silverberg G, Williams MK, Arena JF, Lubs HA, Schwartz CE. Bialer MG, et al. Among authors: schwartz ce. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):491-7. doi: 10.1002/ajmg.1320430173. Am J Med Genet. 1992. PMID: 1605231

8

Relationship between age and IQ among fragile X males: a multicenter study.

Fisch GS, Arinami T, Froster-Iskenius U, Fryns JP, Curfs LM, Borghgraef M, Howard-Peebles PN, Schwartz CE, Simensen RJ, Shapiro LR. Fisch GS, et al. Among authors: schwartz ce. Am J Med Genet. 1991 Feb-Mar;38(2-3):481-7. doi: 10.1002/ajmg.1320380268. Am J Med Genet. 1991. PMID: 2018090

9

Deletion mapping of plasminogen activator inhibitor, type I (PLANH1) and beta-glucuronidase (GUSB) in 7q21----q22.

Schwartz CE, Stanislovitis P, Phelan MC, Klinger K, Taylor HA, Stevenson RE. Schwartz CE, et al. Cytogenet Cell Genet. 1991;56(3-4):152-3. doi: 10.1159/000133073. Cytogenet Cell Genet. 1991. PMID: 2055109

10

Allan-Herndon syndrome. I. Clinical studies.

Stevenson RE, Goodman HO, Schwartz CE, Simensen RJ, McLean WT Jr, Herndon CN. Stevenson RE, et al. Among authors: schwartz ce. Am J Hum Genet. 1990 Sep;47(3):446-53. Am J Hum Genet. 1990. PMID: 2393019 Free PMC article.

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