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Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients. [electronic resource] by
- Chérot, E
- Keren, B
- Dubourg, C
- Carré, W
- Fradin, M
- Lavillaureix, A
- Afenjar, A
- Burglen, L
- Whalen, S
- Charles, P
- Marey, I
- Heide, S
- Jacquette, A
- Heron, D
- Doummar, D
- Rodriguez, D
- Billette de Villemeur, T
- Moutard, M-L
- Guët, A
- Xavier, J
- Périsse, D
- Cohen, D
- Demurger, F
- Quélin, C
- Depienne, C
- Odent, S
- Nava, C
- David, V
- Pasquier, L
- Mignot, C
Producer: 20190911
In:
Clinical genetics vol. 93
Availability: No items available.
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