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Prenatal detection of a 17p11.2 duplication resulting from a rare recombination event and novel PCR-based strategy for molecular identification of Charcot-Marie-Tooth disease type 1A. [electronic resource] by
- Bernard, R
- Labelle, V
- Negre, P
- Tardieu, S
- Azulay, J P
- Malzac, P
- Mattéi, J F
- Leguern, E
- Philip, N
- Lévy, N
Producer: 20000608
In:
European journal of human genetics : EJHG vol. 8
Availability: No items available.
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