Schwartz S - Search Results

1

Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1.

Zinn AR, Tonk VS, Chen Z, Flejter WL, Gardner HA, Guerra R, Kushner H, Schwartz S, Sybert VP, Van Dyke DL, Ross JL. Zinn AR, et al. Among authors: schwartz s. Am J Hum Genet. 1998 Dec;63(6):1757-66. doi: 10.1086/302152. Am J Hum Genet. 1998. PMID: 9837829 Free PMC article.

2

Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.

Wolff DJ, Miller AP, Van Dyke DL, Schwartz S, Willard HF. Wolff DJ, et al. Among authors: schwartz s. Am J Hum Genet. 1996 Jan;58(1):154-60. Am J Hum Genet. 1996. PMID: 8554051 Free PMC article.

3

Deletions in Xq26.3-q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation pattern.

Wolff DJ, Gustashaw KM, Zurcher V, Ko L, White W, Weiss L, Van Dyke DL, Schwartz S, Willard HF. Wolff DJ, et al. Among authors: schwartz s. Hum Genet. 1997 Aug;100(2):256-61. doi: 10.1007/s004390050501. Hum Genet. 1997. PMID: 9254860

4

Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.

Leana-Cox J, Jenkins L, Palmer CG, Plattner R, Sheppard L, Flejter WL, Zackowski J, Tsien F, Schwartz S. Leana-Cox J, et al. Among authors: schwartz s. Am J Hum Genet. 1994 May;54(5):748-56. Am J Hum Genet. 1994. PMID: 8178816 Free PMC article.

5

Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA.

Depinet TW, Zackowski JL, Earnshaw WC, Kaffe S, Sekhon GS, Stallard R, Sullivan BA, Vance GH, Van Dyke DL, Willard HF, Zinn AB, Schwartz S. Depinet TW, et al. Among authors: schwartz s. Hum Mol Genet. 1997 Aug;6(8):1195-204. doi: 10.1093/hmg/6.8.1195. Hum Mol Genet. 1997. PMID: 9259264

6

Analphoid 3qter markers.

Teshima I, Bawle EV, Weksberg R, Shuman C, Van Dyke DL, Schwartz S. Teshima I, et al. Among authors: schwartz s. Am J Med Genet. 2000 Sep 11;94(2):113-9. doi: 10.1002/1096-8628(20000911)94:2<113::aid-ajmg3>3.0.co;2-q. Am J Med Genet. 2000. PMID: 10982967

7

Cytogenetic analysis and construction of a BAC contig across a common neocentromeric region from 9p.

Satinover DL, Vance GH, Van Dyke DL, Schwartz S. Satinover DL, et al. Among authors: schwartz s. Chromosoma. 2001 Aug;110(4):275-83. doi: 10.1007/s004120100143. Chromosoma. 2001. PMID: 11534819

8

Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study.

Graf MD, Christ L, Mascarello JT, Mowrey P, Pettenati M, Stetten G, Storto P, Surti U, Van Dyke DL, Vance GH, Wolff D, Schwartz S. Graf MD, et al. Among authors: schwartz s. J Med Genet. 2006 Aug;43(8):660-4. doi: 10.1136/jmg.2005.037887. J Med Genet. 2006. PMID: 16882740 Free PMC article.

9

The ACMG CYTO2000 subcommittee?

Chen AT, Ing PS, Reidy JA, Schwartz S, Vance GH, Van Dyke DL. Chen AT, et al. Among authors: schwartz s. Genet Med. 1998 Nov-Dec;1(1):67. doi: 10.1097/00125817-199811000-00026. Genet Med. 1998. PMID: 11261434 Free article. No abstract available.

10

Detection of mosaicism in amniotic fluid cultures: a CYTO2000 collaborative study.

Ing PS, Van Dyke DL, Caudill SP, Reidy JA, Bice G, Bieber FR, Buchanan PD, Carroll AJ, Cheung SW, DeWald G, Donahue RP, Gardner HA, Higgins J, Hsu LY, Jamehdor M, Keitges EA, Laundon CH, Luthardt FW, Mascarello J, May KM, Meck JM, Morton C, Patil S, Peakman D, Pettenati MJ, Rao N, Sanger WG, Saxe DF, Schwartz S, Sekhon GS, Vance GH, Wyandt HE, Yu CW, Zenger-Hain J, Chen AT. Ing PS, et al. Among authors: schwartz s. Genet Med. 1999 Mar-Apr;1(3):94-7. doi: 10.1097/00125817-199903000-00006. Genet Med. 1999. PMID: 11336459 Free article.

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