Jonathan Chung to DiGeorge Syndrome
This is a "connection" page, showing publications Jonathan Chung has written about DiGeorge Syndrome.
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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. Circ Cardiovasc Genet. 2017 Oct; 10(5).
Score: 0.149
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Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. Am J Med Genet A. 2012 Nov; 158A(11):2781-7.
Score: 0.106