Kashork CD - Search Results

1

Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases.

Shaffer LG, Kashork CD, Saleki R, Rorem E, Sundin K, Ballif BC, Bejjani BA. Shaffer LG, et al. Among authors: kashork cd. J Pediatr. 2006 Jul;149(1):98-102. doi: 10.1016/j.jpeds.2006.02.006. J Pediatr. 2006. PMID: 16860135

2

Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?

Bejjani BA, Saleki R, Ballif BC, Rorem EA, Sundin K, Theisen A, Kashork CD, Shaffer LG. Bejjani BA, et al. Among authors: kashork cd. Am J Med Genet A. 2005 Apr 30;134(3):259-67. doi: 10.1002/ajmg.a.30621. Am J Med Genet A. 2005. PMID: 15723295

3

Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridization.

Ballif BC, Kashork CD, Saleki R, Rorem E, Sundin K, Bejjani BA, Shaffer LG. Ballif BC, et al. Among authors: kashork cd. Prenat Diagn. 2006 Apr;26(4):333-9. doi: 10.1002/pd.1411. Prenat Diagn. 2006. PMID: 16491513

4

Comparative genomic hybridization by microarray for the detection of cytogenetic imbalance.

Jarmuz M, Ballif BC, Kashork CD, Theisen AP, Bejjani BA, Shaffer LG. Jarmuz M, et al. Among authors: kashork cd. Methods Mol Med. 2006;128:23-31. doi: 10.1007/978-1-59745-159-8_3. Methods Mol Med. 2006. PMID: 17071987

5

Detection of low-level mosaicism by array CGH in routine diagnostic specimens.

Ballif BC, Rorem EA, Sundin K, Lincicum M, Gaskin S, Coppinger J, Kashork CD, Shaffer LG, Bejjani BA. Ballif BC, et al. Among authors: kashork cd. Am J Med Genet A. 2006 Dec 15;140(24):2757-67. doi: 10.1002/ajmg.a.31539. Am J Med Genet A. 2006. PMID: 17103431

6

Rearrangements of chromosome 18 illustrate the utility of array-based comparative genomic hybridization.

Kashork CD, Theisen A, Bejjani BA, Shaffer LG. Kashork CD, et al. Cytogenet Genome Res. 2006;114(3-4):379-83. doi: 10.1159/000094228. Cytogenet Genome Res. 2006. PMID: 16954681

7

Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions.

Yu W, Ballif BC, Kashork CD, Heilstedt HA, Howard LA, Cai WW, White LD, Liu W, Beaudet AL, Bejjani BA, Shaw CA, Shaffer LG. Yu W, et al. Among authors: kashork cd. Hum Mol Genet. 2003 Sep 1;12(17):2145-52. doi: 10.1093/hmg/ddg230. Epub 2003 Jul 15. Hum Mol Genet. 2003. PMID: 12915473

8

Prenatal diagnosis using array CGH.

Kashork CD, Theisen A, Shaffer LG. Kashork CD, et al. Methods Mol Biol. 2008;444:59-69. doi: 10.1007/978-1-59745-066-9_5. Methods Mol Biol. 2008. PMID: 18425472

9

Diagnosis of cryptic chromosomal syndromes by fluorescence in situ hybridization (FISH).

Kashork CD, Theisen A, Shaffer LG. Kashork CD, et al. Curr Protoc Hum Genet. 2010 Oct;Chapter 8:Unit 8.10.1-20. doi: 10.1002/0471142905.hg0810s67. Curr Protoc Hum Genet. 2010. PMID: 20891031

10

The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes.

Shaffer LG, Coppinger J, Morton SA, Alliman S, Burleson J, Traylor R, Walker C, Byerly S, Lamb AN, Schultz R, Ravnan JB, Kashork CD, Torchia BS, Sulpizio S, Sundin K, Schermer M, Adler K, Dallaire S, Ballif BC. Shaffer LG, et al. Among authors: kashork cd. Prenat Diagn. 2011 Aug;31(8):778-87. doi: 10.1002/pd.2766. Epub 2011 Jun 21. Prenat Diagn. 2011. PMID: 21692086

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