-
Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, define pre-malignant neurofibromatosis type 1-associated atypical neurofibromas
Study
phs001993
-
Gene-Environment Interactions (GxE) and Complex Traits
Study
phs001176
-
Gene mutation and rescue in congenital diaphragmatic hernia
Study
phs000485
-
Genetic Epidemiology Network of Arteriopathy (GENOA)
Study
phs001238
-
Aspirin and Inflammation: Mutations, Genes, Pathways and Prevention in Barrett's Esophagus
Study
phs001654
-
National Cancer Institute Clinical and Laboratory Analysis of Familial Cancer
Study
phs001935
-
Analysis of Somatic Mutations in Pediatric AML FAB-M7 Subtype by Whole Transcriptome Sequencing
Study
phs000413
-
Rare Diseases Clinical Research Network (RDCRN) Vasculitis Clinical Research Consortium (VCRC) Longitudinal Protocol for Takayasu's Arteritis
Study
phs000589
-
Exome Sequencing for Diseases of the Immune System: X-linked Immunodeficiency with Magnesium Defect, EBV Infection, and Neoplasia (XMEN)
Study
phs000365
-
The Role of Germline Mutation and Parental Age in Autism Spectrum Disorders
Study
phs001164