40 results on '"Vegter-van der Vlis M"'
Search Results
2. Amyloid B protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch)
3. The Presymptomatic Diagnosis of Huntington’s Disease Using Molecular Techniques, Applications and New Developments
4. Huntington’s Chorea
5. Distress in individuals facing predictive DNA testing for autosomal dominant late-onset disorders: comparing questionnaire results with in-depth interviews
6. [Presymptomatic DNA diagnosis in Huntington's chorea: reactions to the certainty of not being a genetic carrier]
7. Intelligence indices in people with a high/low risk for developing Huntington's disease.
8. Psychological effects of presymptomatic DNA testing for Huntingtonʼs disease in the Dutch program.
9. Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range.
10. Duration of illness in Huntington's disease is not related to age at onset.
11. Age at onset in Huntington's disease: effect of line of inheritance and patient's sex.
12. Paradox of a better test for Huntington's disease.
13. Epidemiological and clinical aspects of hereditary cerebral hemorrhage in Dutch families
14. [Procedure and initial results of presymptomatic DNA studies in Huntington's chorea]
15. PARENTAL TRANSMISSION IN HUNTINGTON'S DISEASE
16. Hereditary cerebral haemorrhage caused by cortical amyloid angiopathy
17. HUNTINGTON'S CHOREA
18. Oculomotor defects in patients with Huntington's disease and their offspring
19. Cognitive and motor functioning in gene carriers for Huntington's disease: a baseline study.
20. Predictability of age at onset in Huntington disease in the Dutch population.
21. Using a roster and haplotyping is useful in risk assessment for persons with intermediate and reduced penetrance alleles in Huntington disease.
22. Predictive testing of 25 percent at-risk individuals for Huntington disease (1987-1997).
23. Two centuries of mortality in ten large families with Huntington disease: a rising impact of gene carriership.
24. Experience in prenatal testing for Huntington's disease in The Netherlands: procedures, results and guidelines (1987-1997).
25. Juvenile Huntington disease in the Netherlands.
26. Presymptomatic DNA testing for Huntington disease: identifying the need for psychological intervention.
27. Defining the proximal border of the Huntington disease candidate region by multipoint recombination analyses.
28. Presymptomatic DNA-testing for Huntington disease: pretest attitudes and expectations of applicants and their partners in the Dutch program.
29. Significant linkage disequilibrium between the Huntington disease gene and the loci D4S10 and D4S95 in the Dutch population.
30. DNA-testing for Huntington's disease in The Netherlands: a retrospective study on psychosocial effects.
31. Presymptomatic, prenatal, and exclusion testing for Huntington disease using seven closely linked DNA markers.
32. Hereditary cerebral haemorrhage with amyloidosis--Dutch type. Magnetic resonance imaging findings in 7 cases.
33. [Procedure and initial results of presymptomatic DNA studies in Huntington's chorea].
34. [Presymptomatic DNA diagnosis in Huntington's chorea: reactions to the certainty of not being a genetic carrier].
35. Genetic linkage studies in Huntington's chorea.
36. Ages of death of children with Huntington's chorea and of their affected parents.
37. Huntington's Chorea in the Netherlands. The problem of genetic heterogeneity.
38. Epidemiological and clinical aspects of hereditary cerebral hemorrhage in Dutch families.
39. Mapping of recombinants near the Huntington disease locus by using G8 (D4S10) and newly isolated markers in the D4S10 region.
40. [Familial cerebral hemorrhage as a result of cerebral amyloid angiopathy].
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