Kashork CD - Search Results

1

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

2

Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure.

Gajecka M, Yu W, Ballif BC, Glotzbach CD, Bailey KA, Shaw CA, Kashork CD, Heilstedt HA, Ansel DA, Theisen A, Rice R, Rice DP, Shaffer LG. Gajecka M, et al. Among authors: kashork cd. Eur J Hum Genet. 2005 Feb;13(2):139-49. doi: 10.1038/sj.ejhg.5201302. Eur J Hum Genet. 2005. PMID: 15483646

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

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

5

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

6

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

7

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

8

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

9

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

10

Partial deletions of the long arm of chromosome 13 associated with holoprosencephaly and the Dandy-Walker malformation.

McCormack WM Jr, Shen JJ, Curry SM, Berend SA, Kashork C, Pinar H, Potocki L, Bejjani BA. McCormack WM Jr, et al. Am J Med Genet. 2002 Nov 1;112(4):384-9. doi: 10.1002/ajmg.10659. Am J Med Genet. 2002. Corrected and republished in: Am J Med Genet A. 2003 Apr 15;118A(2):384-9. PMID: 12376941 Corrected and republished.

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