Results
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29141.
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29151.
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Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology. [electronic resource] by
- Lahbib, Saida
- Leblond, Claire S
- Hamza, Mariem
- Regnault, Béatrice
- Lemée, Laure
- Mathieu, Alexandre
- Jaouadi, Hager
- Mkaouar, Rahma
- Youssef-Turki, Ilhem Ben
- Belhadj, Ahlem
- Kraoua, Ichraf
- Bourgeron, Thomas
- Abdelhak, Sonia
Producer: 20190516
In:
Journal of applied genetics vol. 60
Availability: No items available.
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