Search

Search Constraints

You searched for: Author/Creator Filhol, E

Search Results

1. A study of new NEK8 mutations in patients with severe renal cystic hypodysplasia and ciliopathy-associated defects. Issue 1 (December 2015)

3. Identification of human mutations in TRAF3IP1 in patients with nephronophthisis and retinal degeneration. Issue 1 (December 2015)