Author/Creator: Froyen, G - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Froyen, G

1. 33P Tumour mutational burden ring trial: Evaluation of targeted next-generation sequencing platforms for implementation in clinical practice. (15th December 2019)

Authors:: Lambin, S; Lambrechts, D; De Rop, C; D'Haene, N; Froyen, G; Heukamp, L; Huijsmans, C; Maes, B; Melendez, B; Van Campenhout, C; Vanden Bempt, I; van den Brule, A; Vander Borght, S; Vannuffel, P; Pauwels, P
Journal:: Annals of oncology
Issue:: Volume 30(2019)Supplement 11
Page Start:
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

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

3. High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation. Issue 7 (2nd May 2008)

Authors:: Jehee, F S; Krepischi-Santos, A C V; Rocha, K M; Cavalcanti, D P; Kim, C A; Bertola, D R; Alonso, L G; D'Angelo, C S; Mazzeu, J F; Froyen, G; Lugtenberg, D; Vianna-Morgante, A M; Rosenberg, C; Passos-Bueno, M R
Journal:: Journal of medical genetics
Issue:: Volume 45:Issue 7(2008)
Page Start:: 447
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

4. 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) ↗