Cancer genetics

Bilateral Radial Ray Defects: An Atypical Presentation of 16p11.2 Microdeletion Syndrome

Y Chromosome Microdeletion Detection by Cytoscan HD Microarray Platform

Detection of Copy Number Variations in Breast Cancer Samples Using Single-nucleotide Polymorphism-targeted Massively Multiplexed PCR

Cryptic insertion of 3'FOXO1 into inverted chromosome arm 2q in the presence of two normal chromosome 13s and 13 small interstitial duplications in a patient with alveolar rhabdomyosarcoma

Crizotinib resistance in acute myeloid leukemia with inv(2)(p23q13)/RAN binding protein 2 (RANBP2) anaplastic lymphoma kinase (ALK) fusion and monosomy 7

Congenital Heart Defects in Neonates: Determining the Incidence of Genetic Testing and Follow-up Consultation at UCLA

Concordance of copy number alterations using a common analytic pipeline for genome-wide analysis of Illumina and Affymetrix genotyping data: a report from the Children's Oncology Group

Comprehensive BRCA mutation analysis in the Greek population. Experience from a single clinical diagnostic center

Complex Syndactyly and Atypical Ectrodactyly in a Child with a Mosaic Karyotype Involving Trisomy 21 and Partial Duplication of Chromosome 21

Clinico- and Pathogenomic Analyses of a Single Institution Diffuse Large B-Cell Lymphoma Cohort

Clinical, pathologic, cytogenetic, and molecular profiling in self-identified black women with uterine leiomyomata

Clinical Validation and Implementation of a Targeted Sequencing Panel for Predisposition to Inherited Cancer