Novel ADNP Syndrome Mice Reveal Dramatic Sex-Specific Peripheral Gene Expression With Brain Synaptic and Tau Pathologies - ScienceDirect
Chromatin remodeler Activity-Dependent Neuroprotective Protein (ADNP) contributes to syndromic autism | Clinical Epigenetics | Full Text
The Gene
Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP. - Abstract - Europe PMC
ADNP-HOME
Frontiers | The Eight and a Half Year Journey of Undiagnosed AD: Gene Sequencing and Funding of Advanced Genetic Testing Has Led to Hope and New Beginnings
![Figure 1. [Facial features of individuals with...]. - GeneReviews® - NCBI Bookshelf](https://www.ncbi.nlm.nih.gov/books/NBK355518/bin/adnp-dis-Image001.jpg "Figure 1. [Facial features of individuals with...]. - GeneReviews® - NCBI Bookshelf")
Figure 1. [Facial features of individuals with...]. - GeneReviews® - NCBI Bookshelf
Gene and ADNP protein structure. The region of localization of the... | Download Scientific Diagram
Genie: ADNP Syndrome - Orangesocks.org
ADNP Kids Research Foundation - ADNP Kids Research Foundation
The Gene
Frontiers | The ADNP Syndrome and CP201 (NAP) Potential and Hope
Genes | Free Full-Text | Sensory Reactivity Symptoms Are a Core Feature of ADNP Syndrome Irrespective of Autism Diagnosis
Genes | Free Full-Text | Helsmoortel–Van der Aa Syndrome—Cardiothoracic and Ectodermal Manifestations in Two Patients as Further Support of a Previous Observation on Phenotypic Overlap with RASopathies
Autism and ADNP syndrome: A genetic search and a biomarker discovery | Autism Speaks
Frontal facial photographs of patients. (a–f) Patients 1 (a), 2 (b), 4... | Download Scientific Diagram
A heterozygous microdeletion of 20q13.13 encompassing ADNP gene in a child with Helsmoortel–van der Aa syndrome | European Journal of Human Genetics
CRISPR/Cas9-mediated knockdown to the Adnp gene. (A) A schematic... | Download Scientific Diagram
Artificial intelligence jump starts clinical trial for rare genetic disease - News | UAB
Pictures of children and teeth. (a) Facial pictures: (a 1 ) Picture of... | Download Scientific Diagram
FONDAZIONE TELETHON - Camilla ha sette anni. Ed è affetta da una patologia genetica rara, la sindrome del gene ADNP. La famiglia ha ricevuto la diagnosi grazie al programma malattie rare di
Brain development gene emerges as strong autism candidate | Spectrum | Autism Research News
