-
Metabolism and Genetics of Hypobetalipoproteinemia
Study
phs000561
-
The Genetic Landscape of Mutations in Burkitt Lymphoma
Study
phs000562
-
Rapid Whole Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units
Study
phs000564
-
National Heart, Lung, and Blood Institute (NHLBI) Bench to Bassinet Program: The Pediatric Cardiac Genetics Consortium (PCGC)
Study
phs000571
-
Alzheimer's Disease Sequencing Project (ADSP)
Study
phs000572
-
Genetic Heterogeneity of Diffuse Large B Cell Lymphoma
Study
phs000573
-
Angelman, Rett, Prader-Willi Syndrome Consortium (ARP) Rett Syndrome Natural History Protocol
Study
phs000574
-
Prader-Willi Syndrome and Early-onset Morbid Obesity Natural History Protocol
Study
phs000575
-
Non Dystrophic Myotonias: Genotype-Phenotype Correlation and Longitudinal
Study
phs000578
-
Small Intestine Neuroendocrine Tumors (Carcinoid Tumors)
Study
phs000579
-
Population Architecture using Genomics and Epidemiology (PAGE): Causal Variants Across the Life Course (CALiCo): Strong Heart Study (SHS) and Strong Heart Family Study (SHFS)
Study
phs000580
-
NHLBI GO-ESP: Family Studies (Dilated Cardiomyopathy)
Study
phs000581
-
NHLBI GO-ESP: Family Studies (Familial Interstitial Pneumonia)
Study
phs000582
-
Asian Indian Diabetic Heart Study (AIDHS) /Sikh Diabetes Study (SDS)
Study
phs000583
-
The Longevity Genes Project
Study
phs000584
-
International Consortium for Blood Pressure (ICBP)
Study
phs000585
-
NHLBI GO-ESP: Family Studies (Mendelian Lipid Disorders)
Study
phs000587
-
Screening Protocol and Longitudinal Study of Bone Marrow Failure Syndromes and Cytopenias
Study
phs000592
-
Mucociliary Clearance Consortium (MCC) Rare Genetic Disorders of the Airways: Cross-section Comparison of Clinical Features, and Development of Novel Screening and Genetic Test
Study
phs000595
-
Mucociliary Clearance Consortium (MCC) Longitudinal Study of Primary Ciliary Dyskinesia: Participants 5-18 Years of Age
Study
phs000596
-
DNA Methylation Analysis of Prostate Cancer Cell Lines and Tissues Using Next Generation Sequencing
Study
phs000597
-
Exome Sequencing of Esophageal Adenocarcinoma
Study
phs000598
-
Filtering and Annotation of Variants That Are Rare (FAVR)
Study
phs000601
-
Rare Genetic Steroid Disease Consortium (GSD) Apparent Mineralocorticoid Excess (AME) Syndrome Natural History Clinical Protocol
Study
phs000603
-
Mapping Genes for Mammographic Density
Study
phs000604