Schwartz S - Search Results

1

Child with mosaic variegated aneuploidy and embryonal rhabdomyosarcoma.

Limwongse C, Schwartz S, Bocian M, Robin NH. Limwongse C, et al. Among authors: schwartz s. Am J Med Genet. 1999 Jan 1;82(1):20-4. doi: 10.1002/(sici)1096-8628(19990101)82:1<20::aid-ajmg4>3.0.co;2-5. Am J Med Genet. 1999. PMID: 9916837 Review.

2

Duplication 14(q24.3q31) in a father and daughter: delineation of a possible imprinted region.

Robin NH, Harari-Shacham A, Schwartz S, Wolff DJ. Robin NH, et al. Among authors: schwartz s. Am J Med Genet. 1997 Aug 22;71(3):361-5. doi: 10.1002/(sici)1096-8628(19970822)71:3<361::aid-ajmg20>3.0.co;2-h. Am J Med Genet. 1997. PMID: 9268110

3

Adult with an interstitial deletion of chromosome 10 [del(10)(q25. 1q25.3)]: overlap with Coffin-Lowry syndrome.

McCandless SE, Schwartz S, Morrison S, Garlapati K, Robin NH. McCandless SE, et al. Among authors: schwartz s. Am J Med Genet. 2000 Nov 13;95(2):93-8. doi: 10.1002/1096-8628(20001113)95:2<93::aid-ajmg1>3.0.co;2-b. Am J Med Genet. 2000. PMID: 11078556

4

Molecular characterization and delineation of subtle deletions in de novo "balanced" chromosomal rearrangements.

Kumar A, Becker LA, Depinet TW, Haren JM, Kurtz CL, Robin NH, Cassidy SB, Wolff DJ, Schwartz S. Kumar A, et al. Among authors: schwartz s. Hum Genet. 1998 Aug;103(2):173-8. doi: 10.1007/pl00008706. Hum Genet. 1998. PMID: 9760201

5

Molecular refinement of karyotype: beyond the cytogenetic band.

Sirko-Osadsa DA, Cassidy SB, Depinet TW, Robin NH, Limwongse C, Schwartz S. Sirko-Osadsa DA, et al. Among authors: schwartz s. Genet Med. 1999 Sep-Oct;1(6):254-61. doi: 10.1097/00125817-199909000-00003. Genet Med. 1999. PMID: 11258626 Free article.

6

Distal 5q deletion syndrome: phenotypic correlations.

Schafer IA, Robin NH, Posch JJ, Clark BA, Izumo S, Schwartz S. Schafer IA, et al. Among authors: schwartz s. Am J Med Genet. 2001 Sep 15;103(1):63-8. doi: 10.1002/ajmg.1513. Am J Med Genet. 2001. PMID: 11562936 Review.

7

Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndrome.

Tsuchiya KD, Wiesner G, Cassidy SB, Limwongse C, Boyle JT, Schwartz S. Tsuchiya KD, et al. Among authors: schwartz s. Genes Chromosomes Cancer. 1998 Feb;21(2):113-8. doi: 10.1002/(sici)1098-2264(199802)21:2<113::aid-gcc6>3.0.co;2-3. Genes Chromosomes Cancer. 1998. PMID: 9491322

8

Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes.

Crowe CA, Schwartz S, Black CJ, Jaswaney V. Crowe CA, et al. Among authors: schwartz s. Am J Med Genet. 1997 Sep 5;71(4):406-13. Am J Med Genet. 1997. PMID: 9286446 Review.

9

Uniparental isodisomy 13 in a normal female due to transmission of a maternal t(13q13q).

Stallard R, Krueger S, James RS, Schwartz S. Stallard R, et al. Among authors: schwartz s. Am J Med Genet. 1995 May 22;57(1):14-8. doi: 10.1002/ajmg.1320570105. Am J Med Genet. 1995. PMID: 7645591

10

Congenital central hypoventilation syndrome: mutation analysis of the receptor tyrosine kinase RET.

Bolk S, Angrist M, Schwartz S, Silvestri JM, Weese-Mayer DE, Chakravarti A. Bolk S, et al. Among authors: schwartz s. Am J Med Genet. 1996 Jun 28;63(4):603-9. doi: 10.1002/(SICI)1096-8628(19960628)63:4<603::AID-AJMG14>3.0.CO;2-M. Am J Med Genet. 1996. PMID: 8826440

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