Schwartz S - Search Results

1

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

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

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.

4

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.

5

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.

6

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

7

Parental origin of De Novo chromosome 9 deletions in del(9p) syndrome.

Micale MA, Haren JM, Conroy JM, Crowe CA, Schwartz S. Micale MA, et al. Among authors: schwartz s. Am J Med Genet. 1995 May 22;57(1):79-81. doi: 10.1002/ajmg.1320570118. Am J Med Genet. 1995. PMID: 7645605

8

Molecular cytogenetics of a de novo interstitial deletion of chromosome arm 6q in a developmentally normal girl.

Kumar A, Cassidy SB, Romero L, Schwartz S. Kumar A, et al. Among authors: schwartz s. Am J Med Genet. 1999 Sep 17;86(3):227-31. doi: 10.1002/(sici)1096-8628(19990917)86:3<227::aid-ajmg6>3.0.co;2-3. Am J Med Genet. 1999. PMID: 10482870

9

Betaine-homocysteine methyltransferase-2: cDNA cloning, gene sequence, physical mapping, and expression of the human and mouse genes.

Chadwick LH, McCandless SE, Silverman GL, Schwartz S, Westaway D, Nadeau JH. Chadwick LH, et al. Among authors: schwartz s. Genomics. 2000 Nov 15;70(1):66-73. doi: 10.1006/geno.2000.6319. Genomics. 2000. PMID: 11087663

10

Proximal interstitial deletion of 7q: a case report and review of the literature.

Zackowski JL, Raffel LJ, Blank CA, Schwartz S. Zackowski JL, et al. Among authors: schwartz s. Am J Med Genet. 1990 Jul;36(3):328-32. doi: 10.1002/ajmg.1320360317. Am J Med Genet. 1990. PMID: 2194394 Review.

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