Schwartz CE - Search Results

1

Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21.

Schwartz CE, Ulmer J, Brown A, Pancoast I, Goodman HO, Stevenson RE. Schwartz CE, et al. Am J Hum Genet. 1990 Sep;47(3):454-8. Am J Hum Genet. 1990. PMID: 2393020 Free PMC article.

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

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

5

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

6

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

7

Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome.

Suthers GK, Mulley JC, Voelckel MA, Dahl N, Väisänen ML, Steinbach P, Glass IA, Schwartz CE, van Oost BA, Thibodeau SN, et al. Suthers GK, et al. Among authors: schwartz ce. Am J Hum Genet. 1991 Mar;48(3):460-7. Am J Hum Genet. 1991. PMID: 1671806 Free PMC article.

8

DNA fingerprinting: the utilization of minisatellite probes to detect a somatic mutation in the proteus syndrome.

Schwartz CE, Brown AM, Der Kaloustian VM, McGill JJ, Saul RA. Schwartz CE, et al. EXS. 1991;58:95-105. doi: 10.1007/978-3-0348-7312-3_7. EXS. 1991. PMID: 1831169

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

Localization of the Miller-Dieker critical region is proximal to locus D17S34 (p144D6) in 17p13.3.

Schwartz CE, Sauer SM, Brown AM, Divelbiss JE, Patil SR. Schwartz CE, et al. Genomics. 1990 Aug;7(4):621-4. doi: 10.1016/0888-7543(90)90208-c. Genomics. 1990. PMID: 2387588

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