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Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia. [electronic resource] by
- Tekin, M
- Oztürkmen Akay, H
- Fitoz, S
- Birnbaum, S
- Cengiz, F B
- Sennaroğlu, L
- Incesulu, A
- Yüksel Konuk, E B
- Hasanefendioğlu Bayrak, A
- Sentürk, S
- Cebeci, I
- Utine, G E
- Tunçbilek, E
- Nance, W E
- Duman, D
Producer: 20080723
In:
Clinical genetics vol. 73
Availability: No items available.
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50.
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Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome. [electronic resource] by
- Riazuddin, Saima
- Ahmed, Zubair M
- Hegde, Rashmi S
- Khan, Shaheen N
- Nasir, Idrees
- Shaukat, Uzma
- Riazuddin, Sheikh
- Butman, John A
- Griffith, Andrew J
- Friedman, Thomas B
- Choi, Byung Yoon
Producer: 20110426
In:
BMC medical genetics vol. 12
Availability: No items available.
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