Search Results (24)
Click the Why column to see why an item matched the search.
| Match | Type | Why |
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| Complex Reoperation in a Patient With DiGeorge Syndrome. | Academic Article |
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| Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome. | Academic Article |
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| Genetic Drivers of Kidney Defects in the DiGeorge Syndrome. | Academic Article |
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| DiGeorge Syndrome | Concept |
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| Imamoto, Akira | Person |
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| Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome. | Academic Article |
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| Essential role of the Crk family-dosage in DiGeorge-like anomaly and metabolic homeostasis. | Academic Article |
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| Evidence that duplications of 22q11.2 protect against schizophrenia. | Academic Article |
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| Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder. | Academic Article |
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| 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 |
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| Mosaicism del(22)(q11.2q11.2)/dup(22)(q11.2q11.2) in a patient with features of 22q11.2 deletion syndrome. | Academic Article |
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| Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. | Academic Article |
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| The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans. | Academic Article |
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| Chaney, Mark | Person |
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| Crkl deficiency disrupts Fgf8 signaling in a mouse model of 22q11 deletion syndromes. | Academic Article |
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