Canlyniadau Chwilio - Redon, R

NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome gan Borck, G, Redon, R, Sanlaville, D, Rio, M, Prieur, M, Lyonnet, S, Vekemans, M, Carter, N, Munnich, A, Colleaux, L, Cormier-Daire, V

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Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation... gan Shaw-Smith, C, Redon, R, Rickman, L, Rio, M, Willatt, L, Fiegler, H, Firth, H, Sanlaville, D, Winter, R, Colleaux, L, Bobrow, M, Carter, N

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Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: contiguous gene deletion or "deletion with positional effect" syndrome? gan Redon, R, Rio, M, Gregory, S, Cooper, R, Fiegler, H, Sanlaville, D, Banerjee, R, Scott, C, Carr, P, Langford, C, Cormier-Daire, V, Munnich, A, Carter, N, Colleaux, L

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Array‐based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders gan Jacquemont, M‐L, Sanlaville, D, Redon, R, Raoul, O, Cormier‐Daire, V, Lyonnet, S, Amiel, J, Merrer, M Le, Heron, D, de Blois, M‐C, Prieur, M, Vekemans, M, Carter, N P, Munnich, A, Colleaux, L, Philippe, A

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