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.