Home
About
Overview
Sharing Data
ORCID
Help
History (9)
The Theory of Ultra-Coarse-Graining. 1. General Principles.
Naja naja
Requirements for contractility in disordered cytoskeletal bundles.
Spatially resolved quantification of oxygen consumption rate in ex vivo lymph node slices.
Reduced NADPH oxidase type 2 activity mediates sleep fragmentation-induced effects on TC1 tumors in mice.
See All 9 Pages
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
Search Results (16)
More Search Options
Match
Type
Why
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.
Academic Article
Why?
Complex Reoperation in a Patient With DiGeorge Syndrome.
Academic Article
Why?
Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome.
Academic Article
Why?
Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation.
Academic Article
Why?
Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome.
Academic Article
Why?
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.
Academic Article
Why?
Mosaicism del(22)(q11.2q11.2)/dup(22)(q11.2q11.2) in a patient with features of 22q11.2 deletion syndrome.
Academic Article
Why?
Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients.
Academic Article
Why?
Essential role of the Crk family-dosage in DiGeorge-like anomaly and metabolic homeostasis.
Academic Article
Why?
Evidence that duplications of 22q11.2 protect against schizophrenia.
Academic Article
Why?
Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder.
Academic Article
Why?
The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans.
Academic Article
Why?
Crkl deficiency disrupts Fgf8 signaling in a mouse model of 22q11 deletion syndromes.
Academic Article
Why?
Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome.
Academic Article
Why?
Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes.
Academic Article
Why?
Per Page
15
25
50
100
Page
of 2
Next
Prev
Search Criteria
DiGeorge Syndrome
Filter by Type
All
(27)
People
(10)
Research
(16)
Concepts
(1)
_
Click "Why?" to see why an item matched the search.