Finding the difference: de novo mutations in schizophrenia | Beyond the Ion Channel
De novo mutations in autism
De novo mutations in isolated RP patients. A: De novo mutation in... | Download Scientific Diagram
De novo mutations in folate-related genes associated with common developmental disorders - ScienceDirect
Post-zygotic Point Mutations Are an Underrecognized Source of De Novo Genomic Variation - ScienceDirect
Epileptic encephalopathies: de novo mutations take center stage | Beyond the Ion Channel
New insights into the generation and role of de novo mutations in health and disease | Genome Biology | Full Text
De novo mutations in human genetic disease | Nature Reviews Genetics
De Novo Synonymous Mutations in Regulatory Elements Contribute to the Genetic Etiology of Autism and Schizophrenia | Semantic Scholar
De Novo Mutations Reflect Development and Aging of the Human Germline: Trends in Genetics
Frontiers | De novo Mutations (DNMs) in Autism Spectrum Disorder (ASD): Pathway and Network Analysis
Types of sporadic gene mutations leading to disease. (a, b) De novo... | Download Scientific Diagram
De novo mutations in human genetic disease | Nature Reviews Genetics
denovo-DB
What is a de novo mutation? Find out below! | By SPARK for AutismFacebook
A de novo mutation in the NALCN gene in an adult patient with cerebellar ataxia associated with intellectual disability and arthrogryposis - Wang - 2016 - Clinical Genetics - Wiley Online Library
New insights into the generation and role of de novo mutations in health and disease | Genome Biology | Full Text
De novo mutation in NALCN. A: Pictures of the patient and of one of her... | Download Scientific Diagram
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder | Science
NEJM on X: "De novo mutation — Any DNA sequence change that occurs during replication, such as a gene alteration newly occurring in a family as a result of a DNA sequence
Genes | Free Full-Text | Somatic Mosaicism in the Human Genome
Neuropsychiatric De novo Mutations Database
Hereditary spherocytosis: Genetics
