NGS Identifies Rare Disease Variants in Infants with Undiagnosed Disease
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More Expectant Parents to Get Access to Non-Invasive Prenatal Testing
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Genomic Insights in Rare Disease Webinar Series
Illumina alums launch Cradle Genomics with $17.1M for first-trimester fetal DNA testing | Fierce Biotech
Illumina and Children's Hospital of Fudan in China
TruSight Oncology 500 Selected to Power Liquid Biopsy Studies
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Rapid Genome Sequencing of Critically Ill Children
CSRWire - Illuminating Rare Disease: Get to Know SLC6A1 Connect
How Illumina Creates a Culture of Care through Robust Employee Benefits and Wellness Programs | News Direct
VIDEO: One Couple's Struggle with Infertility
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Exome Sequencing Reveals Misdiagnoses in Epidermolysis Bullosa Patients
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Illumina, German hospital team up for genome sequencing to test genetic disease in kids | Seeking Alpha
Brotman Baty Institute Collaborates with Illumina and GeneDx on Whole-Genome Sequencing Study to Support Families of Children with Developmental Differences | Brotman Baty Institute
Children drowned one day before relatives to get custody | cbs8.com
Newborn Genomic Screening: In Sickness and In Health
