Maximizing the Detection of Copy Number Variants in the Highly Homologous Deafness-Infertility Syndrome Locus in Standard-of-care Testing

Minjie Luo^{1

2}, Laura K Conlin^{1

2}, Ramakrishnan Rajagopalan^{1

2}

Affiliations

¹ Department of Pathology and Laboratory Medicine, Division of Genomic Diagnostics, Children's Hospital of Philadelphia, United States.
² Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, United States.

Editorial

Minjie Luo et al. Clin Chem. 2023.

. 2023 Jun 1;69(6):545-547.

doi: 10.1093/clinchem/hvad044.

Minjie Luo^{1

2}, Laura K Conlin^{1

2}, Ramakrishnan Rajagopalan^{1

2}

¹ Department of Pathology and Laboratory Medicine, Division of Genomic Diagnostics, Children's Hospital of Philadelphia, United States.
² Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, United States.

No abstract available

Comment on

Leveraging Unique Chromosomal Microarray Probes to Accurately Detect Copy Number at the Highly Homologous 15q15.3 Deafness-Infertility Syndrome Locus.
Sack LM, Mertens L, Murphy E, Hutchinson L, Giersch ABS, Mason-Suares H. Sack LM, et al. Clin Chem. 2023 Jun 1;69(6):583-594. doi: 10.1093/clinchem/hvad032. Clin Chem. 2023. PMID: 37022747