Mutations in the human SIX3 gene in holoprosencephaly are loss of function
Hum. Mol. Genet. Domené et al. 17: 3919
Supplementary Data
Supplementary Data
Files in this Data Supplement:
- Supplementary Data - Supplementary Data
- Supplementary Table 1 - Supplementary Table 1
- Supplementary Table 2 - Supplementary Table 2