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NIPA2
Variable Penetrance of the 15Q11.2 BP1–BP2 Microduplication in a Family With
Chromosomal Microarray Analysis in Turkish Patients with Unexplained Developmental Delay and Intellectual Developmental Disorders
In Silico Cancer Cell Versus Stroma Cellularity
Rabbit Anti-NIPA-2 Antibody-SL7465R
BMC Genomics Biomed Central
Magnesium Supplement and the 15Q11.2 BP1–BP2 Microdeletion (Burnside–Butler) Syndrome: a Potential Treatment?
Content Based Search in Gene Expression Databases and a Meta-Analysis of Host Responses to Infection
(Burnside-Butler) Syndrome in Five Families
Microduplications at the 15Q11.2 BP1–BP2 Locus Are Enriched in Patients with Anorexia Nervosa T
Methylation-Specific Multiplex Ligation-Dependent Probe
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Milger Et Al. Pulmonary CCR2+CD4+ T Cells Are Immune Regulatory And
PWS Publications Apr to Jun 2020 PWS PAPERS of INTEREST
Genetic Dissection Identifies Necdin As a Driver Gene in a Mouse Model
Segmental Duplications Promote Genomic Instability In
TRANSPOSABLE ELEMENTS OCCUR MORE FREQUENTLY in AUTISM RISK GENES: Emily L
NIPA2 (T-12): Sc-79659
Comparison Between Timelines of Transcriptional Regulation in Mammals, Birds, and Teleost Fish Somitogenesis
Top View
NIPA2 Rabbit Pab Antibody
Integrative Multi-Omic Analysis Identifies New Drivers and Pathways
Genome-Wide DNA Methylation and Gene Expression Analyses In
15Q11.2 Microduplications
Characterization of a Chromosome Rearrangement Associated with Cardiopathy and Autism”, by Sara Melo Dias
PWS Publications Apr to Jun 2019 PWS PAPERS of INTEREST
Neuroscore: a Genome-Wide Omics-Based Model to Identify Candidate Disease Genes of the Central Nervous System
(Burnside-Butler) Syndrome
The 15Q11.2 BP1-BP2 Microdeletion
Copy Number Variations in a Cohort of 420 Individuals with Neurodevelopmental Disorders from the South of Brazil
15Q11.2 Microdeletions
Genes, Chromosomes and Disease
Maternal Protein Restriction in Rats Alters the Expression of Genes Involved in Mitochondrial Metabolism and Epitranscriptomics in Fetal Hypothalamus
Unique and Atypical Deletions in Prader&Ndash;Willi Syndrome Reveal Distinct Phenotypes
(AVIELA) for Gene Expression Prof
A Cross-Disorder Dosage Sensitivity Map of the Human Genome
Familial 15Q11.2 Micro Deletions Are Not Fully Penetrant in Two Cases
Low Dose Radiation Response Curves, Networks and Pathways in Human Lymphoblastoid