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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?
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.Academic Article Why?
DiGeorge SyndromeConcept Why?
Imamoto, AkiraPerson Why?
Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome.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?
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?
The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans.Academic Article Why?
Chaney, MarkPerson Why?
Crkl deficiency disrupts Fgf8 signaling in a mouse model of 22q11 deletion syndromes.Academic Article Why?
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