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Author/Creator Redon, R

1. Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders. Issue 11 (13th July 2006)

Authors:
Jacquemont, M-L; Sanlaville, D; Redon, R; Raoul, O; Cormier-Daire, V; Lyonnet, S; Amiel, J; Le Merrer, M; Heron, D; de Blois, M-C; Prieur, M; Vekemans, M; Carter, N P; Munnich, A; Colleaux, L; Philippe, A
Journal:
Journal of medical genetics
Issue:
Volume 43:Issue 11(2006)
Page Start:
843
Record Type:
Journal Article
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2. Genome-wide association study identifies 18 new susceptibility variants loci associated with Brugada Syndrome. (25th November 2020)

Authors:
Barc, J; Trados, R; Glinge, C; Simonet, F; Chiang, D; Jouni, M; Jurgens, S; The Brugada Syndrome Genetic Consortium, B.R.S; Tanck, M; Dina, C; Probst, V; Wilde, A; Redon, R; Schott, J.J; Bezzina, C
Journal:
European heart journal
Issue:
Volume 41:(2020)Supplement 2
Page Start:
Record Type:
Journal Article
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3. Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features. Issue 4 (1st April 2004)

Authors:
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 P
Journal:
Journal of medical genetics
Issue:
Volume 41:Issue 4(2004)
Page Start:
241
Record Type:
Journal Article
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5. P336Exome sequencing of multiple affected individuals from an Irish family with Brugada Syndrome uncovers a novel locus for the disorder. (15th July 2014)

Authors:
Barc, J G; Marsman, RF; Marsman, RF; Le Scouarnec, S; Le Scouarnec, S; Mizusawa, Y; Mizusawa, Y; Lindenbaum, P; Lindenbaum, P; Carter, N; Carter, N; Redon, R; Redon, R; Wilde, AAM; Wilde, AAM; Mckeown, P; Mckeown, P; Bezzina, CR; Bezzina, CR
Journal:
Cardiovascular research
Issue:
Volume 103(2014)Supplement 1
Page Start:
S61
Record Type:
Journal Article
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6. Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: contiguous gene deletion or "deletion with positional effect" syndrome?. Issue 2 (2nd February 2005)

Authors:
Redon, R; Rio, M; Gregory, S G; Cooper, R A; Fiegler, H; Sanlaville, D; Banerjee, R; Scott, C; Carr, P; Langford, C; Cormier-Daire, V; Munnich, A; Carter, N P; Colleaux, L
Journal:
Journal of medical genetics
Issue:
Volume 42:Issue 2(2005)
Page Start:
166
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗