In the Line-Up: Deleted Genes Associated With DiGeorge/22q11.2 Deletion Syndrome: Are They All Suspects?

Journal of Neurodevelopmental Disorders - United Kingdom
doi 10.1186/s11689-019-9267-z
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

DiGeorge Syndrome (Chromosome 22q11.2 Deletion Syndrome): A Historical Perspective With Review of 66 Patients

Journal of Surgery and Medicine
2019English

Sclerocornea Associated With the Chromosome 22q11.2 Deletion Syndrome

American Journal of Medical Genetics, Part A
Genetics
2008English

22q11.2 Deletion Syndrome-Associated Parkinson's Disease

Movement Disorders Clinical Practice
Neurology
2018English

All-Cause Mortality and Survival in Adults With 22q11.2 Deletion Syndrome

Genetics in Medicine
MedicineGenetics
2019English

A Novel 22q11.2 Microdeletion in DiGeorge Syndrome

American Journal of Human Genetics
Genetics
1999English

Candidate Modifier Genes for Immune Function in 22q11.2 Deletion Syndrome

Molecular genetics & genomic medicine
GeneticsMolecular Biology
2019English

Obesity in Adults With 22q11.2 Deletion Syndrome

Genetics in Medicine
MedicineGenetics
2016English

Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome

American Journal of Human Genetics
Genetics
2015English

Complement Activation in 22q11.2 Deletion Syndrome

Journal of Clinical Immunology
AllergyImmunology
2020English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy