Last data update: Sep 15, 2021. (Total: 3468 publications since 2011)
|Query Trace: all>>Deborah Koontz[CDC Author]|
| MALDI-TOF-MS Assay to Detect the Hemizygous 22q11.2 Deletion in DNA from Dried Blood Spots.
Lisa J Kobrynski, Golriz K Yazdanpanah, Deborah Koontz, Francis K Lee, and Robert F Vogt
Clinical chemistry 2015 Nov
Similar articles in PubMed DOI:10.1373/clinchem.2015.247148
| A pyrosequencing-based assay for the rapid detection of the 22q11.2 deletion in DNA from buccal and dried blood spot samples.
Deborah Koontz, Kirsten Baecher, Lisa Kobrynski, Stanimila Nikolova, and Margaret Gallagher
J Mol Diagn 2014 Sep 16(5) 533-40
Similar articles in PubMed DOI:10.1016/j.jmoldx.2014.05.003
| Prothrombin G20210A mutation is associated with young-onset stroke: the genetics of early-onset stroke study and meta-analysis.
Baijia Jiang, Kathleen A Ryan, Ali Hamedani, Yuching Cheng, Mary J Sparks, Deborah Koontz, Christopher J Bean, Margaret Gallagher, W Craig Hooper, Patrick F McArdle, Jeffrey R O'Connell, O Colin Stine, Marcella A Wozniak, Barney J Stern, Braxton D Mitchell, Steven J Kittner, and John W Cole
Stroke 2014 Apr 45(4) 961-7
Similar articles in PubMed DOI:10.1161/STROKEAHA.113.004063
| Folate-related gene variants in Irish families affected by neural tube defects.
Ridgely Fisk Green, Julianne Byrne, Krista S Crider, Margaret Gallagher, Deborah Koontz, and Robert J Berry
Frontiers in genetics 2013 4223
Similar articles in PubMed DOI:10.3389/fgene.2013.00223
| Evaluation of mailed pediatric buccal cytobrushes for use in a case-control study of birth defects.
Margaret L Gallagher, Cynthia Sturchio, Ashley Smith, Deborah Koontz, Mary M Jenkins, Margaret A Honein, and Sonja A Rasmussen
Birth Defects Res. Part A Clin. Mol. Teratol. 2011 Jul 91(7) 642-8
Similar articles in PubMed DOI:10.1002/bdra.20829