Paired Tumor-Normal Sequencing Identifies a Homozygous Pathogenic BRCA2 Germline Variant Leading to a Diagnosis of an Atypical Presentation of Fanconi Anemia
Homozygosity for the SMN2 c.859G>C Allele Accounts for the Phenotypic and Genotypic Discordances Seen in an Uncommon Case of Spinal Muscular Atrophy Revealed by Newborn Screening
Identification of Streptococcus intermedius Associated With Culture-Negative Brain Abscesses and Meningoencephalitis Through CSF Metagenomic Sequencing
Ethical Frontiers: The Promise and Perils of Healthcare AI in a Socially Connected World
Location: Grand Ballroom, Level 3
Plenary Speaker: Takunda Matose, PHD, MBe (he/him/his) – Cincinnati Children's Hospital and Medical Center/ University of Cincinnati College of Medicine
Recommendations for Clinical Molecular Laboratories for Detection of Homologous Recombination Deficiency in Cancer: A Joint Consensus Recommendation of the Association of Molecular Pathology, Association of Cancer Care Centers, and College of American Pathologists
Recommendations for Clinical Molecular Laboratories for Detection of Homologous Recombination Deficiency in Cancer: A Joint Consensus Recommendation of the Association of Molecular Pathology, Association of Cancer Care Centers, and College of American Pathologists
Recommendations for Clinical Molecular Laboratories for Detection of Homologous Recombination Deficiency in Cancer: A Joint Consensus Recommendation of the Association of Molecular Pathology, Association of Cancer Care Centers, and College of American Pathologists