Hasil Pencarian - Farshid Parvini
- Menampilkan 1 - 5 hasil dari 5
-
1
-
2
A novel recessive PDZD7 bi-allelic mutation in an Iranian family with non-syndromic hearing loss oleh Hossein Fahimi, Samira Behroozi, Sadaf Noavar, Farshid Parvini
Diterbitkan 2021-02-01
Artikel -
3
-
4
-
5