Condition: Goldenhar Syndrome


rs3754648 in AGAP1 gene and Goldenhar Syndrome PMID 26853712 2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.

rs10459648 in ARID3B gene and Goldenhar Syndrome PMID 26853712 2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.

rs4750407 in FRMD4A gene and Goldenhar Syndrome PMID 26853712 2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.

rs17802111 in LOC101926974 gene and Goldenhar Syndrome PMID 26853712 2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.

rs17090300 in LOC107984024;LINC00393;LINC00392 gene and Goldenhar Syndrome PMID 26853712 2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.

rs754423 in NID2 gene and Goldenhar Syndrome PMID 26853712 2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.

rs7420812 in PARD3B gene and Goldenhar Syndrome PMID 26853712 2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.

rs3923380 in SHROOM3 gene and Goldenhar Syndrome PMID 26853712 2016 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.