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ZNF385D
Whole-Genome Microarray Detects Deletions and Loss of Heterozygosity of Chromosome 3 Occurring Exclusively in Metastasizing Uveal Melanoma
A Chromosome Level Genome of Astyanax Mexicanus Surface Fish for Comparing Population
MOCHI Enables Discovery of Heterogeneous Interactome Modules in 3D Nucleome
Genome-Wide Association Scan Identifies New Variants Associated
Genome-Wide Insights on Gastrointestinal Nematode
Genome-Wide Association Scan Identifies
Genetic Epidemiology of Hypertension in Populations
BCL9 and C9orf5 Are Associated with Negative Symptoms in Schizophrenia: Meta-Analysis of Two Genome-Wide Association Studies
Downloaded from Ensembl
Deciphering Common and Rare Genetic E Ects on Reading Ability
10Th Anniversary of the Human Genome Project
Application of Gene Network Analysis Techniques Identifies AXIN1/PDIA2 and Endoglin Haplotypes Associated with Bicuspid Aortic Valve
Investigating the Effects of Copy Number Variants on Reading and Language Performance Alessandro Gialluisi1,2, Alessia Visconti3, Erik G
Genetics of Cognitive Trajectory in Brazilians: 15 Years of Follow-Up from the Bambuí-Epigen Cohort Study of Aging Mateus H
Predicting Developmental Dyslexia: a Brief Review of Genetics, Language and the Brain Michael J Figuccio*
Identification of Critical Genetic Variants Associated with Metabolic
MOCHI Enables Discovery of Heterogeneous Interactome Modules in 3D Nucleome
The Polygenic Nature and Complex Genetic Architecture of Specific
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Association Between Genes Regulating Neural Pathways for Quantitative Traits of Speech and Language Disorders