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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?
Imamoto, AkiraPerson Why?
DiGeorge SyndromeConcept 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?
Chaney, MarkPerson Why?
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