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Author/Creator de Blois, M-C

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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Available online (eLD content is only available in our Reading Rooms) ↗

2. Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation. Issue 4 (1st April 2002)

Authors:
Rio, M; Molinari, F; Heuertz, S; Ozilou, C; Gosset, P; Raoul, O; Cormier-Daire, V; Amiel, J; Lyonnet, S; Le Merrer, M; Turleau, C; de Blois, M-C; Prieur, M; Romana, S; Vekemans, M; Munnich, A; Colleaux, L
Journal:
Journal of medical genetics
Issue:
Volume 39:Issue 4(2002)
Page Start:
266
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Genotype–phenotype correlation of 30 patients with Smith-Magenis syndrome (SMS) using comparative genome hybridisation array: cleft palate in SMS is associated with larger deletions. Issue 8 (27th April 2007)

Authors:
Andrieux, J; Villenet, C; Quief, S; Lignon, S; Geffroy, S; Roumier, C; de Leersnyder, H; de Blois, M-C; Manouvrier, S; Delobel, B; Benzacken, B; Bitoun, P; Attie-Bitach, T; Thomas, S; Lyonnet, S; Vekemans, M; Kerckaert, J-P
Journal:
Journal of medical genetics
Issue:
Volume 44:Issue 8(2007)
Page Start:
537
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗