Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Reza Asadollahi
Dosage Changes of MED13L Further Delineate Its Role in Congenital Heart Defects and Intellectual Disability
European Journal of Human Genetics
Genetics
Low-Level Chromosomal Mosaicism in Neurodevelopmental Disorders
Molecular Syndromology
Genetics
Related publications
Brachydactyly-Mesomelia-Intellectual Disability-Heart Defects Syndrome
Heterozygous Loss-Of-Function Variants of MEIS2 Cause a Triad of Palatal Defects, Congenital Heart Defects, and Intellectual Disability
European Journal of Human Genetics
Genetics
MED13L-related Intellectual Disability: Involvement of Missense Variants and Delineation of the Phenotype
Neurogenetics
Molecular Neuroscience
Genetics
Cellular
Recurrence of Congenital Heart Defects in Families
Circulation
Cardiovascular Medicine
Physiology
Cardiology
Severe Intellectual Disability Associated With Recessive Defects in CNTNAP2 and NRXN1
Molecular Syndromology
Genetics
Copy Number Variation in Congenital Heart Defects
Current Genetic Medicine Reports
Comprehensive Approach to Congenital Heart Defects
Journal of Cardiovascular Disease Research
Cardiovascular Medicine
Cardiology
MESP1 Mutations in Patients With Congenital Heart Defects
Human Mutation
Genetics
What Is New in Genetics of Congenital Heart Defects?
Frontiers in Pediatrics
Child Health
Pediatrics
Perinatology