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1. Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain

2. Computational and molecular approaches for predicting unreported causal missense mutations in Belgian patients with haemophilia A

3. The 'royal disease'--haemophilia A or B? A haematological mystery is finally solved

4. PP6.1 – 2162 Hamartin and tuberin expression studies: further insights into TSC1 and TSC2 genes in a cohort of patients with well defined phenotype

5. Prevalence and Spectrum of SDHx Mutations in Pheochromocytoma and Paraganglioma in Patients from Belgium: An Update.

6. Accessibility and visibility of genetic testing for haemophilia across Europe: Where do we stand?

7. Genetic mosaicism in haemophilia: A practical review to help evaluate the risk of transmitting the disease.

8. Inhibitor epidemiology and genetic-related risk factors in people with haemophilia from Côte d'Ivoire.

9. Incidental finding of unreported large duplication in F8 gene during prenatal analysis: Which management for genetic counselling?

10. Review of molecular mechanisms at distal Xq28 leading to balanced or unbalanced genomic rearrangements and their phenotypic impacts on hemophilia.

13. Principles of genetic variations and molecular diseases: applications in hemophilia A.

14. Five int22h homologous copies at the Xq28 locus identified in intron22 inversion type 3 of the Factor VIII gene.

15. Tandem inversion duplication within F8 Intron 1 associated with mild haemophilia A.

16. Overrepresentation of missense mutations in mild hemophilia A patients from Belgium: founder effect or independent occurrence?

17. Intron 22 homologous regions are implicated in exons 1-22 duplications of the F8 gene.

18. Functional assessment of TSC2 variants identified in individuals with tuberous sclerosis complex.

19. Computational and molecular approaches for predicting unreported causal missense mutations in Belgian patients with haemophilia A.

20. The 'royal disease'--haemophilia A or B? A haematological mystery is finally solved.

21. Identification of de novo deletion in the factor VIII gene by MLPA technique in two girls with isolated factor VIII deficiency.

22. CF gene and cystic fibrosis transmembrane conductance regulator expression in autosomal dominant polycystic kidney disease.

23. Novel germline mutations in the APC gene and their phenotypic spectrum in familial adenomatous polyposis kindreds.

24. Isolated polycystic liver disease as a distinct genetic disease, unlinked to polycystic kidney disease 1 and polycystic kidney disease 2.

25. The genetic background of familial adenomatous polyposis. Linkage analysis, the APC gene identification and mutation screening.

26. High CTG repeat number in nodular thyroid tissue from a myotonic dystrophy patient.

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