| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | A novel GLI3c.750delC truncation mutation in a multiplex Greig cephalopolysyndactyly syndrome family with an unusual phenotypic combination in a patient. | Meta Gene | 2014 | 0.75 |
| 2 | GLI3 mutations in syndromic and non-syndromic polydactyly in two Indian families. | Congenit Anom (Kyoto) | 2016 | 0.75 |