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Investigation of the Causal Etiology in a Patient with T-B+NK+ Immunodeficiency
Study
phs002990
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Parallel CRISPR Editing of Familial ALS Mutations Into a Healthy Control iPSC Line
Study
phs002440
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Genetic Analysis of Limb Malformation Disorders: Freeman Sheldon Syndrome Exome Sequencing Study (LMD-FSS)
Study
phs000204
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Genomic Analysis of Extra-Nodal Natural Killer/T-Cell Lymphoma (ENKTCL)
Study
phs002925
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The Spatio-Temporal Evolution of Multiple Myeloma from Baseline to Relapse-Refractory States
Study
phs002625
-
Personalized Breast Cancer Vaccines Based on Genome Sequencing
Study
phs002787
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Reference Standards for Mosaic Variant Detection
Study
phs003399
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The Genomic Landscape of Interval Colorectal Cancers
Study
phs003093
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PIEZO1 Loss of Function Compound Heterozygous Mutation in the Rare Congenital Human Disorder Prune Belly Syndrome
Study
phs003475
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The Genetic Evolution of Acral Melanoma
Study
phs003451