Genome-wide CRISPR-Cas9 screen analyzed by SLIDER identifies network of repressor complexes that regulate TRIM24 - ScienceDirect
IMPE Abstracts | IMPE Abstracts
PDF) A review of genetic syndromes associated with hypertrichosis
speech disorder - Ontology Browser - Rat Genome Database
De Novo Variants in CNOT1, a Central Component of the CCR4-NOT Complex Involved in Gene Expression and RNA and Protein Stability
De novo variants in CNOT9 cause a neurodevelopmental disorder with or without epilepsy - ScienceDirect
New Genetic Mutations Linked to Autism Spectrum Disorder Uncovered by Scientists
Rolf Bodmer, Ph.D. | Sanford Burnham Prebys
Metabolic Disorders | NGS Panels: centogene.com
Issues · DiseaseOntology/HumanDiseaseOntology · GitHub
Biallelic PAN2 variants in individuals with a syndromic neurodevelopmental disorder and multiple congenital anomalies | European Journal of Human Genetics
Journal of Inherited Metabolic Disease: Vol 38, No 3
CNOT1 Gene - GeneCards | CNOT1 Protein | CNOT1 Antibody
Psph Mouse Gene Details | phosphoserine phosphatase | International Mouse Phenotyping Consortium
Chromosome mapping of selected 4p deletions, including present cases,... | Download Scientific Diagram
Machteld M Oud's research works | Radboud University Medical Centre (Radboudumc), Nijmegen and other places
3billion - Hello, how are you today? We've got 4 new rare... | Facebook
Biallelic PAN2 variants in individuals with a syndromic neurodevelopmental disorder and multiple congenital anomalies | European Journal of Human Genetics
CNOT1 Gene - GeneCards | CNOT1 Protein | CNOT1 Antibody
Frontiers | Biological Therapy in Primary Sjögren's Syndrome: Effect on Salivary Gland Function and Inflammation
VISSERS-BODMER SYNDROME - Ontology Browser - Rat Genome Database
Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder - ScienceDirect
Myrthe van den Born's research works | Erasmus University Rotterdam, Rotterdam (EUR) and other places
