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High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease. [electronic resource] by
- Bilir, B
- Yapici, Z
- Yalcinkaya, C
- Baris, I
- Carvalho, C M B
- Bartnik, M
- Ozes, B
- Eraksoy, M
- Lupski, J R
- Battaloglu, E
Producer: 20130712
In:
Clinical genetics vol. 83
Availability: No items available.
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11.
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A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis. [electronic resource] by
- Baris, I
- Arisoy, A E
- Smith, A
- Agostini, M
- Mitchell, C S
- Park, S M
- Halefoglu, A M
- Zengin, E
- Chatterjee, V K
- Battaloglu, E
Producer: 20061113
In:
The Journal of clinical endocrinology and metabolism vol. 91
Availability: No items available.
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12.
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Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second gene. [electronic resource] by
- Bissar-Tadmouri, N
- Nelis, E
- Züchner, S
- Parman, Y
- Deymeer, F
- Serdaroglu, P
- De Jonghe, P
- Van Gerwen, V
- Timmerman, V
- Schröder, J M
- Battaloglu, E
Producer: 20040903
In:
Neurology vol. 62
Availability: No items available.
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13.
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PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia. [electronic resource] by
- Ozes, B
- Karagoz, N
- Schüle, R
- Rebelo, A
- Sobrido, M-J
- Harmuth, F
- Synofzik, M
- Pascual, S I P
- Colak, M
- Ciftci-Kavaklioglu, B
- Kara, B
- Ordóñez-Ugalde, A
- Quintáns, B
- Gonzalez, M A
- Soysal, A
- Zuchner, S
- Battaloglu, E
Producer: 20180528
In:
Clinical genetics vol. 92
Availability: No items available.
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