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Author/Creator Marynen, P

2. A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients. Issue 1 (1st January 2003)

Authors:
Longo, I; Frints, S G M; Fryns, J-P; Meloni, I; Pescucci, C; Ariani, F; Borghgraef, M; Raynaud, M; Marynen, P; Schwartz, C; Renieri, A; Froyen, G
Journal:
Journal of medical genetics
Issue:
Volume 40:Issue 1(2003)
Page Start:
11
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports. Issue 8 (20th February 2006)

Authors:
Menten, B; Maas, N; Thienpont, B; Buysse, K; Vandesompele, J; Melotte, C; de Ravel, T; Van Vooren, S; Balikova, I; Backx, L; Janssens, S; De Paepe, A; De Moor, B; Moreau, Y; Marynen, P; Fryns, J-P; Mortier, G; Devriendt, K; Speleman, F; Vermeesch, J R
Journal:
Journal of medical genetics
Issue:
Volume 43:Issue 8(2006)
Page Start:
625
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

7. Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype map. Issue 9 (1st September 2004)

Authors:
Van Buggenhout, G; Melotte, C; Dutta, B; Froyen, G; Van Hummelen, P; Marynen, P; Matthijs, G; de Ravel, T; Devriendt, K; Fryns, J P; Vermeesch, J R
Journal:
Journal of medical genetics
Issue:
Volume 41:Issue 9(2004)
Page Start:
691
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗