|?|| (A;A) (A;G) (G;G) ||28|
] Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate
[PMID 18571626] RASD2, MYH9, and CACNG2 genes at chromosome 22q12 associated with the subgroup of schizophrenia with non-deficit in sustained attention and executive function.
[PMID 18716610] Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate.
[PMID 20124285] Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.