BASAL CELL NEVUS (GORLIN) SYNDROME WITH A NOVEL HETEROZYGOUS DELETION FRAMESHIFT MUTATION (C.959DELC, P.VAL322 PHE FSX2) IN THE PTCH1 GENE ASSOCIATED WITH EPIRETINAL MEMBRANE, ODONTOGENIC KERATOCYSTS AND WITHOUT SKIN LESIONS AND FALX CEREBRI CALCIFICATION için istatistikler
Toplam ziyaret
| views | |
|---|---|
| BASAL CELL NEVUS (GORLIN) SYNDROME WITH A NOVEL HETEROZYGOUS DELETION FRAMESHIFT MUTATION (C.959DELC, P.VAL322 PHE FSX2) IN THE PTCH1 GENE ASSOCIATED WITH EPIRETINAL MEMBRANE, ODONTOGENIC KERATOCYSTS AND WITHOUT SKIN LESIONS AND FALX CEREBRI CALCIFICATION | 0 |
Aylık toplam ziyaret
| views | |
|---|---|
| Ocak 2025 | 0 |
| Şubat 2025 | 0 |
| Mart 2025 | 0 |
| Nisan 2025 | 0 |
| Mayıs 2025 | 0 |
| Haziran 2025 | 0 |
| Temmuz 2025 | 0 |
