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X-linked Alport syndrome in Hellenic families: phenotypic heterogeneity and mutations near interruptions of the collagen domain in COL4A5. [electronic resource] by
- Demosthenous, P
- Voskarides, K
- Stylianou, K
- Hadjigavriel, M
- Arsali, M
- Patsias, C
- Georgaki, E
- Zirogiannis, P
- Stavrou, C
- Daphnis, E
- Pierides, A
- Deltas, C
Producer: 20120808
In:
Clinical genetics vol. 81
Availability: No items available.
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Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis. [electronic resource] by
- Papazachariou, L
- Papagregoriou, G
- Hadjipanagi, D
- Demosthenous, P
- Voskarides, K
- Koutsofti, C
- Stylianou, K
- Ioannou, P
- Xydakis, D
- Tzanakis, I
- Papadaki, A
- Kallivretakis, N
- Nikolakakis, N
- Perysinaki, G
- Gale, D P
- Diamantopoulos, A
- Goudas, P
- Goumenos, D
- Soloukides, A
- Boletis, I
- Melexopoulou, C
- Georgaki, E
- Frysira, E
- Komianou, F
- Grekas, D
- Paliouras, C
- Alivanis, P
- Vergoulas, G
- Pierides, A
- Daphnis, E
- Deltas, C
Producer: 20180528
In:
Clinical genetics vol. 92
Availability: No items available.
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