(Q34309519)
Statements
1 reference
VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells (English)
1 reference
Elena V Semina
1 reference
Helen A Mintz-Hittner
1 reference
Laura J Frishman
1 reference
Thomas C Prager
1 reference
Jeffrey C Murray
1 reference
1 April 2004
1 reference
1 reference
111
1 reference
4
1 reference
828-836
1 reference
Identifiers
1 reference
1 reference