Genome study reveals patterns and properties of human de novo mutations
Large scale variation in the rate of germ-line de novo mutation, base composition, divergence and diversity in humans | PLOS Genetics
Finding the difference: de novo mutations in schizophrenia | Beyond the Ion Channel
De novo mutations in isolated RP patients. A: De novo mutation in... | Download Scientific Diagram
Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pair | Journal of Medical Genetics
Hereditary spherocytosis: Genetics
Frontiers | De novo Mutations (DNMs) in Autism Spectrum Disorder (ASD): Pathway and Network Analysis
Multisite de novo mutations in human offspring after paternal exposure to ionizing radiation | Scientific Reports
The role of de novo mutations in adult-onset neurodegenerative disorders | SpringerLink
TADA – a joint analysis of de novo and inherited risk factors in autism | Beyond the Ion Channel
Solved 3. Examine the accompanying pedigree and determine | Chegg.com
New insights into the generation and role of de novo mutations in health and disease | Genome Biology | Full Text
New insights into the generation and role of de novo mutations in health and disease | Genome Biology | Full Text
Germline mutation - Wikipedia
De novo - Definition and Examples | Biology Online
What is KAT6A? | kat6a
De Novo Mutations Reflect Development and Aging of the Human Germline: Trends in Genetics
De novo mutations in autism
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
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder | Science
De Novo Truncating Mutations in AHDC1 in Individuals with Syndromic Expressive Language Delay, Hypotonia, and Sleep Apnea - ScienceDirect
The role of de novo mutations in adult-onset neurodegenerative disorders | SpringerLink
denovo-DB
