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Whole Genome Sequencing of Familial Non-Medullary Thyroid Cancer Identifies Germline Alterations in MAPK/ERK and PI3K/AKT Signaling Pathways
Human Social Genomics in the Multi-Ethnic Study of Atherosclerosis
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E. M. G. Campbell, D. Nonneman and G. A. Rohrer Chromosome 8 Fine Mapping a Quantitative Trait Locus Affecting Ovulation Rate In
The Conserved DNMT1 Dependent Methylation Regions in Human Cells Are Vulnerable to Environmental Rotenone
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PDE1A Polymorphism Contributes to the Susceptibility
Forward Genomics of a Complex Trait: Mammalian Basal Metabolic Rate
Diagnosis of Familial Wolf-Hirschhorn Syndrome Due to a Paternal Cryptic Chromosomal Rearrangement by Conventional and Molecular Cytogenetic Techniques
Tracking Profiles of Genomic Instability in Spontaneous Transformation and Tumorigenesis Lesley Lawrenson Wayne State University
Analysis of the Whole Genome Sequence
Divergence in Alternative Polyadenylation Contributes to Gene
Prelamin a Influences a Program of Gene Expression in Regulation of Cell Cycle Control Christina N
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Autosomal Recessive Variants in Intellectual Disability and Autism Spectrum Disorder
Whole-Genome Resequencing of Wild and Domestic Sheep Identifies
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Analysis of Astroglial Secretomic Profile in the Mecp2-Deficient Male
RNA Sequencing Unravels the Genetics of Refractory/Relapsed T-Cell Acute Lymphoblastic Leukemia