Condition: MECKEL SYNDROME, TYPE 10


rs757863670 in B9D2 gene and MECKEL SYNDROME, TYPE 10 PMID 26092869 2015 Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity.

rs750436680 in B9D2;TGFB1 gene and MECKEL SYNDROME, TYPE 10 PMID 26092869 2015 Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity.