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2. Fluorescence in situ hybridization analysis of 110 hematopoietic disorders with chromosome 5 abnormalities: do de novo and therapy-related myelodysplastic syndrome–acute myeloid leukemia actually differ?

5. Identification of symbol digit modality test score extremes in Huntington's disease

7. ONLINE MUTATION REPORT

9. 25 ans de l’association polypose adénomate familiale belge : résultats et enseignements d’un registre national

11. Suicidal ideation in a European Huntington's disease population

13. The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients

14. Use of topiramate in relation to the risk of orofacial clefts

16. Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY

17. NMDA receptor gene variations as modifiers in Huntington disease: a replication study

19. Observing Huntington's Disease: the European Huntington's Disease Network's REGISTRY

20. Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease

21. EuroBioBank (EBB): European Network of DNA, Cell and Tissue Banks for Rare Diseases

22. β-Defensin Genomic Copy Number Does Not Influence the Age of Onset in Huntington's Disease

23. Discrepancies in reporting the CAG repeat lengths for Huntington's disease

24. NMDA receptor gene variations as modifiers in Huntington disease

27. A new familial short stature syndrome: Brussels type

29. IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS Sign

30. CNGA3 mutations in hereditary cone photoreceptor disorders

33. Allelic heterogeneity of SMARD1 at the IGHMBP2 locus

34. A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2)

36. A Spectrum of Mutations in the Second Gene for Autosomal Dominant Polycystic Kidney Disease (PKD2)

40. Frequency of cystic fibrosis transmembrane conductance regulator gene mutations and 5T allele in patients with allergic bronchopulmonary aspergillosis.

43. Hematological malignancies with a deletion of 11q23: cytogenetic and clinical aspects. European 11q23 Workshop participants.

48. Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy.

49. Orofacial clefting: Update on the role of genetics

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