Publications by authors named "Loretta W Mahon"

10Publications

Effects of platforms, size filter cutoffs, and targeted regions of cytogenomic microarray on detection of copy number variants and uniparental disomy in prenatal diagnosis: Results from 5026 pregnancies.

Prenat Diagn 2019 02 8;39(3):137-156. Epub 2019 Feb 8.

Cytogenetics and Genomics, Quest Diagnostics Nichols Institute, San Juan Capistrano, California.

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http://dx.doi.org/10.1002/pd.5375DOI Listing
February 2019

Interstitial Chromosome 3p14.1 Deletion due to a Maternal Insertion: Phenotype and Association with Balanced Parental Rearrangement.

Mol Syndromol 2016 Apr 16;7(1):43-8. Epub 2016 Mar 16.

Division of Medical Genetics, Department of Pediatrics, Cedars-Sinai Medical Center, San Juan Capistrano, Calif., USA; Department of Pediatrics, David Geffen School of Medicine at UCLA, Los Angeles, Calif., USA.

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http://dx.doi.org/10.1159/000444603DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4862392PMC
April 2016