Schwartz CE - Search Results

1

Obstetrical and gynecological complications in fragile X carriers: a multicenter study.

Schwartz CE, Dean J, Howard-Peebles PN, Bugge M, Mikkelsen M, Tommerup N, Hull C, Hagerman R, Holden JJ, Stevenson RE. Schwartz CE, et al. Am J Med Genet. 1994 Jul 15;51(4):400-2. doi: 10.1002/ajmg.1320510419. Am J Med Genet. 1994. PMID: 7943006

2

Evidence of founder chromosomes in fragile X syndrome.

Richards RI, Holman K, Friend K, Kremer E, Hillen D, Staples A, Brown WT, Goonewardena P, Tarleton J, Schwartz C, et al. Richards RI, et al. Nat Genet. 1992 Jul;1(4):257-60. doi: 10.1038/ng0792-257. Nat Genet. 1992. PMID: 1302021

3

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.

4

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.

5

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

6

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

7

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

8

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

9

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

10

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

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