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MP2PRT: Comprehensive Genomic Profiling to Identify Alterations Associated with Relapse for NCI Standard Risk (SR) B-Lineage ALL and NCI High Risk (HR) B-Lineage ALL with Favorable Genetic Features
Study
phs002005
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Lobular Carcinomas In Situ Display Intra-Lesion Genetic Heterogeneity and Clonal Evolution in the Progression to Invasive Disease
Study
phs001006
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Bone Microarchitecture
Study
phs002102
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Disease Variant Landscape of a Large Multiethnic Population of Moyamoya Patients by Exome Sequencing
Study
phs001700
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NHLBI and NIDDK Sponsored GWAS in Benign Ethnic Neutropenia/Leukopenia (BEN) in African-Americans (age >45 yrs old) from the REGARDS
Study
phs000507
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Genetics of Cutaneous T-Cell Lymphoma
Study
phs001877
-
CIP: Obesity-Diabetes Familial Risk, Viva La Familia Study
Study
phs000616
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99 Cases of Small Cell Lung Cancer Study
Study
phs001083
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Whole Exome Sequencing of Uveal Melanoma
Study
phs001370
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Inherited Genetic Variation and Predisposition to Testicular Germ Cell Tumor: UPenn Local TGCT Study
Study
phs001307