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Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum. [electronic resource] by
- Caglayan, A O
- Per, H
- Akgumus, G
- Gumus, H
- Baranoski, J
- Canpolat, M
- Calik, M
- Yikilmaz, A
- Bilguvar, K
- Kumandas, S
- Gunel, M
Producer: 20140408
In:
Clinical genetics vol. 84
Availability: No items available.
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12.
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Lack of serum antineuronal antibodies in children with autism. [electronic resource] by
- Bayram, A K
- Kardas, F
- Demirci, E O
- Gokahmetoglu, S
- Ozmen, S
- Canpolat, M
- Oztop, D B
- Kumandas, S
- Gumus, H
- Per, H
Producer: 20160421
In:
Bratislavske lekarske listy vol. 117
Availability: No items available.
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