Submicroscopic deletions at 22q11.2: Variability of the clinical picture and delineation of a commonly deleted region
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference24 articles.
1. Isolation of a zinc finger gene consistently deleted in DiGeorge syndrome
2. Di George syndrome and 22q11 rearrangements
3. Chromosomal assignment of human YAC clones by fluorescence in Situ hybridization: Use of single-yeast-colony PCR and multiple labeling
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2. Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndrome;Birth Defects Research;2020-05-20
3. Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects;American Journal of Medical Genetics Part A;2018-10
4. Cortical Dysconnectivity Measured by Structural Covariance Is Associated With the Presence of Psychotic Symptoms in 22q11.2 Deletion Syndrome;Biological Psychiatry: Cognitive Neuroscience and Neuroimaging;2018-05
5. Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3;Circulation: Cardiovascular Genetics;2017-10
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