1. Comparative study of the prevalence of clotting factor deficiency in carriers of haemophilia A and haemophilia B. Issue 5 (9th July 2017) Authors: Boban, A.; Lambert, C.; Lannoy, N.; Hermans, C. Journal: Haemophilia Issue: Volume 23:Issue 5(2017) Page Start: e471 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Five int22h homologous copies at the Xq28 locus identified in intron22 inversion type 3 of the Factor VIII gene. (January 2016) Authors: Lannoy, N.; Ravoet, M.; Grisart, B.; Fretigny, M.; Vikkula, M.; Hermans, C. Journal: Thrombosis research Issue: Volume 137(2016) Page Start: 224 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Five int22h homologous copies at the Xq28 locus identified in intron22 inversion type 3 of the Factor VIII gene. (January 2016) Authors: Lannoy, N.; Ravoet, M.; Grisart, B.; Fretigny, M.; Vikkula, M.; Hermans, C. Journal: Thrombosis research Issue: Volume 137(2016) Page Start: 224 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Incidental finding of unreported large duplication in F8 gene during prenatal analysis: Which management for genetic counselling?. Issue 182 (October 2019) Authors: Lannoy, N.; Lambert, C.; Van Damme, A.; Hermans, C. Journal: Thrombosis research Issue: Issue 182(2019) Page Start: 39 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Medium grain niobium SRF cavity production technology for science frontiers and accelerator applications. (1st April 2023) Authors: Myneni, G.; Ciovati, G.; Dhakal, P.; Rimmer, R.A.; Khanal, B.D.; Dohmae, T.; Saeki, T.; Umemori, K.; Yamanaka, M.; Michizono, S.; Carl, M.; Fajardo, A.; Lannoy, N.; Elsayed-Ali, H.E.; Islam, Md O.; Sayeed, Md N.; Kumar, A.; Yamamoto, A. Journal: Journal of instrumentation Issue: Volume 18:Number 4(2023) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Overrepresentation of missense mutations in mild hemophilia A patients from Belgium: founder effect or independent occurrence?. Issue 6 (June 2015) Authors: Lannoy, N.; Lambert, C.; Vikkula, M.; Hermans, C. Journal: Thrombosis research Issue: Volume 135:Issue 6(2015) Page Start: 1057 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Principles of genetic variations and molecular diseases: applications in hemophilia A. (August 2016) Authors: Lannoy, N.; Hermans, C. Journal: Critical reviews in oncology/hematology Issue: Volume 104(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Principles of genetic variations and molecular diseases: applications in hemophilia A. (August 2016) Authors: Lannoy, N.; Hermans, C. Journal: Critical reviews in oncology/hematology Issue: Volume 104(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Review of molecular mechanisms at distal Xq28 leading to balanced or unbalanced genomic rearrangements and their phenotypic impacts on hemophilia. Issue 5 (8th August 2018) Authors: Lannoy, N.; Hermans, C. Journal: Haemophilia Issue: Volume 24:Issue 5(2018) Page Start: 711 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Tandem inversion duplication within F8 Intron 1 associated with mild haemophilia A. (11th May 2015) Authors: Lannoy, N.; Bandelier, C.; Grisart, B.; Reginster, M.; Ronge‐Collard, E.; Vikkula, M.; Hermans, C. Journal: Haemophilia Issue: Volume 21:Number 4(2015:Jul.) Page Start: 516 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗