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COG8
Genome-Wide Copy Number Variant Analysis For
Targeted Polymerase Chain Reaction-Based Enrichment and Next Generation Sequencing for Diagnostic Testing of Congenital Disorders of Glycosylation Melanie A
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Genome-Wide Insights on Gastrointestinal Nematode
Molecular Cytogenetic Characterization of Partial Monosomy 2P and Trisomy 16Q in a Newborn: a Case Report
Genomic Approach in Idiopathic Intellectual Disability Maria De Fátima E Costa Torres
Agricultural University of Athens
393LN V 393P 344SQ V 393P Probe Set Entrez Gene
1 Genome-Wide CRISPR-Cas9 Screen Reveals Common Factors in Dsrna and Sindbis Virus
COG8 (NM 032382) Human Untagged Clone – SC108150 | Origene
Coexpression Networks Based on Natural Variation in Human Gene Expression at Baseline and Under Stress
Identification of Molecular Tumor Markers in Renal Cell Carcinomas with TFE3 Protein Expression by RNA Sequencing
S41467-019-13965-X.Pdf
And Post-Synaptic Abnormalities in Schizophrenia Lynsey S
Genetic Parameters and Associated Genomic Regions for Global
Nutrigenomics Approach Elucidates Health-Promoting Effects of High Vegetable Intake in Lean and Obese Men
Genome-Wide Analysis of Epigenetics and Alternative Promoters in Cancer Cells
Identification of Molecular Tumor Markers in Renal Cell Carcinomas
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A Comprehensive Survey of Non-Canonical Splice Sites in the Human Transcriptome Guillermo E
Modelado Integrativo De La Estructura 3D De Macromoléculas
Detecting Gene Modules Differentially Expressed in Multiple Human Brain
Chromosomal Mapping and Phenotypic Characterization of Hereditary Otosclerosis Linked to the OTSC4 Locus
The Interactome of the Copper Transporter ATP7A Belongs to A
Multi-Level Proteomics Reveals Host-Perturbation Strategies Of
Chromosome-Specific and Global Effects of Aneuploidy In
A Comprehensive Survey of Non-Canonical Splice Sites in the Human Transcriptome Guillermo E
Viewed As a Transcription Silencing Mechanism [11, 12]
Exome Sequencing Analysis of Rare Autosomal Recessive Disorders
Ggdonto Ontology As a Knowledge-Base for Genetic
Congenital Disorders of Glycosylation: an Update on Defects Affecting the Biosynthesis of Dolichol-Linked Oligosaccharides
Characterization and Therapy of Congenital Disorders of Glycosylation
Genome-Wide Copy Number Variant Analysis for Congenital Ventricular Septal Defects in Chinese Han Population