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Documentation of fertility preservation discussions for young adults with cancer: Examining compliance with treatment guidelines
Impact of a Clinical Trial Initiative on Clinical Trial Enrollment in a Multidisciplinary Prostate Cancer Clinic

High-Throughput Sequencing in Respiratory, Critical Care, and Sleep Medicine Research. An Official American Thoracic Society Workshop Report
Inhibition of Human DNA Polymerases Eta and Kappa by Indole-Derived Molecules Occurs through Distinct Mechanisms

The Epigenetic Regulation of Wound Healing
Palingol: a declarative programming language to describe nucleic acids' secondary structures and to scan sequence database.

Hodgkin Lymphoma, Version 2.2015: Clinical Practice Guidelines in Oncology
Fertility care in the era of commercial direct-to-consumer home DNA kits: issues to ponder

Human maternal heritage in Andalusia (Spain): its composition reveals high internal complexity and distinctive influences of mtDNA haplogroups U6 and L in the western and eastern side of region
Efficiency, error and yield in light-directed maskless synthesis of DNA microarrays

Efficiency, error and yield in light-directed maskless synthesis of DNA microarrays
DNA-damage response network at the crossroads of cell-cycle checkpoints, cellular senescence and apoptosis

Disparities in Genetic Testing and Care among Black women with Hereditary Breast Cancer
Poster Session A

T-wave alternans in a case with systemic lupus erythematosus-related myocarditis
Using the class 1 integron-integrase gene as a proxy for anthropogenic pollution

Detection of Epidemic USA300 Community-Associated Methicillin-Resistant Staphylococcus aureus Strains by Use of a Single Allele-Specific PCR Assay Targeting a Novel Polymorphism of Staphylococcus aureus pbp3
Comparison of molecular testing modalities for detection of ROS1 rearrangements in a cohort of positive patient samples

Can molecular biomarkers replace a clinical risk score for resectable colorectal liver metastasis?
A patient with features of albright hereditory osteodystrophy and unusual neuropsychiatric findings without coding Gsalpha mutations

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