Cardiofaciocutaneous Syndrome With Rare Structural Variant in DOCK8 Gene Associated With Neurodevelopmental Disorders

Clinical Case Reports - United Kingdom
doi 10.1002/ccr3.2729
Full Text
Abstract

Available in full text

Categories
Medicine
Date
Authors
Publisher

Wiley

Related search

A YWHAZ Variant Associated With Cardiofaciocutaneous Syndrome Activates the RAF-ERK Pathway

Frontiers in Physiology
Physiology
2019English

Genetic Variant Rs17225178 in the ARNT2 Gene Is Associated With Asperger Syndrome

Molecular Autism
PsychiatryMental HealthDevelopmental NeuroscienceDevelopmental BiologyMolecular Biology
2015English

Rare NonconservativeLRP6Mutations Are Associated With Metabolic Syndrome

Human Mutation
Genetics
2013English

Dermatological Manifestations in Cardiofaciocutaneous Syndrome

British Journal of Dermatology
DermatologyMedicine
2019English

Verbal Fluency Test in Children With Neurodevelopmental Disorders

Journal of Neurosciences in Rural Practice
NeuroscienceNeurology
2020English

Connecting the CNTNAP2 Networks With Neurodevelopmental Disorders

Molecular Syndromology
Genetics
2015English

The Functional Variant Rs334558 of GSK3B Is Associated With Remission in Patients With Depressive Disorders

Pharmacogenomics and Personalized Medicine
Molecular MedicinePharmacology
2018English

The IL-1Ra Gene Variable Number Tandem Repeat Variant Is Associated With Susceptibility to Temporomandibular Disorders in Turkish Population

Journal of Clinical Laboratory Analysis
AllergyImmunologyBiochemistryPublic HealthMedical Laboratory TechnologyClinical BiochemistryHematologyMicrobiologyEnvironmentalOccupational Health
2017English

Are Structural Brain Abnormalities Associated With Suicidal Behavior in Patients With Psychotic Disorders?

Journal of Psychiatric Research
PsychiatryBiological PsychiatryMental Health
2013English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy