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MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype. [electronic resource] by
- Smol, T
- Petit, F
- Piton, A
- Keren, B
- Sanlaville, D
- Afenjar, A
- Baker, S
- Bedoukian, E C
- Bhoj, E J
- Bonneau, D
- Boudry-Labis, E
- Bouquillon, S
- Boute-Benejean, O
- Caumes, R
- Chatron, N
- Colson, C
- Coubes, C
- Coutton, C
- Devillard, F
- Dieux-Coeslier, A
- Doco-Fenzy, M
- Ewans, L J
- Faivre, L
- Fassi, E
- Field, M
- Fournier, C
- Francannet, C
- Genevieve, D
- Giurgea, I
- Goldenberg, A
- Green, A K
- Guerrot, A M
- Heron, D
- Isidor, B
- Keena, B A
- Krock, B L
- Kuentz, P
- Lapi, E
- Le Meur, N
- Lesca, G
- Li, D
- Marey, I
- Mignot, C
- Nava, C
- Nesbitt, A
- Nicolas, G
- Roche-Lestienne, C
- Roscioli, T
- Satre, V
- Santani, A
- Stefanova, M
- Steinwall Larsen, S
- Saugier-Veber, P
- Picker-Minh, S
- Thuillier, C
- Verloes, A
- Vieville, G
- Wenzel, M
- Willems, M
- Whalen, S
- Zarate, Y A
- Ziegler, A
- Manouvrier-Hanu, S
- Kalscheuer, V M
- Gerard, B
- Ghoumid, Jamal
Producer: 20190926
In:
Neurogenetics vol. 19
Availability: No items available.
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