353 results on '"Ten Kate, Leo"'
Search Results
2. First steps in exploring prospective exome sequencing of consanguineous couples
3. Consanguinity and Endogamy in the Netherlands : Demographic and Medical Genetic Aspects
4. Discharge and Farewell
5. Community Genetics : A Bridge between Clinical Genetics and Public Health
6. Community Genetics
7. How Should Preconceptional Cystic Fibrosis Carrier Screening Be Provided? Opinions of Potential Providers and the Target Population
8. Offering Preconceptional Cystic Fibrosis Carrier Couple Screening in the Absence of Established Preconceptional Care Services
9. Editorial
10. Editorial
11. Community Genetics in The Netherlands
12. Editorial
13. Educational priorities and current involvement in genetic practice: a survey of midwives in the Netherlands, UK and Sweden
14. Editorial
15. Explorative Study of Costs, Effects and Savings of Screening for Female Fragile X Premutation and Full Mutation Carriers in the General Population
16. Genetic risk
17. A short history of the first 3 years of the Community Genetics Network and its newsletter
18. Confidence of primary care physicians in their ability to carry out basic medical genetic tasks—a European survey in five countries—Part 1
19. Comparison of Single-Entry and Double-Entry Two-Step Couple Screening for Cystic Fibrosis Carriers
20. General practitioner management of genetic aspects of a cardiac disease: a scenario-based study to anticipate providers’ practices
21. Autosomal recessive disease in children of consanguineous parents: inferences from the proportion of compound heterozygotes
22. Community genetics. Its definition 2010
23. Preconceptionele screening op dragerschap voor cystische fibrose: Implementatiemogelijkheden en barrières
24. Editorial: genetic aspects of preconception consultation in primary care
25. Preconceptional genetic carrier testing and the commercial offer directly-to-consumers
26. TP53 germline mutation testing in 180 families suspected of Li–Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes
27. Relative frequencies of cystic fibrosis mutations in The Netherlands as an illustration of significant regional variation in a small country
28. Does informed decision making influence psychological outcomes after receiving a positive screening outcome?
29. Haplotype identity between individuals who share a CFTR mutation allele “identical by descent”: demonstration of the usefulness of the haplotype-sharing concept for gene mapping in real populations
30. Does offering and performing prenatal screening influence womenʼs attachment to their unborn child? A longitudinal randomized controlled trial
31. Does prenatal screening influence anxiety levels of pregnant women? A longitudinal randomised controlled trial
32. Down syndrome: effects of demographic factors and prenatal diagnosis on the future livebirth prevalence
33. Is there a link between personalized medicine and community genetics?
34. Community genetics in the Netherlands
35. Birth and population prevalence of Duchenne muscular dystrophy in the Netherlands
36. Parental origin and germline mosaicism of deletions and duplications of the dystrophin gene: a European study
37. The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas
38. Current practice and future interest of GPs and prospective parents in pre-conception care in The Netherlands
39. Attitudes of Potential Providers Towards Preconceptional Cystic Fibrosis Carrier Screening
40. Psychomotor developmental delay and epilepsy in an offspring of father–daughter incest: quantification of the causality probability
41. Mutations in the gene for methylenetetrahydrofolate reductase, homocysteine levels, and vitamin status in women with a history of preeclampsia
42. Comparison of activities and attitudes of general practitioners concerning genetic counseling over a 10-year time-span
43. Challenges in the care for consanguineous couples: an exploratory interview study among general practitioners and midwives
44. Validation of the determination of ΔF508 mutations of the cystic fibrosis gene in over 11000 mouthwashes
45. Do consanguineous parents of a child affected by an autosomal recessive disease have more DNA identical-by-descent than similarly-related parents with healthy offspring? Design of a case-control study
46. Screening for cystic fibrosis and its evaluation
47. The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol
48. Second cousins with cystic fibrosis and no common ancestor who is a carrier
49. Cost of care of patients with cystic fibrosis in The Netherlands in 1990-1
50. Frequency of the ΔF508 mutation and XV2c,KM19 haplotypes in cystic fibrosis families from The Netherlands: haplotypes without ΔF508 still in disequilibrium
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.