| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Association of DD genotype of angiotensin-converting enzyme gene (I/D) polymorphism with hypertension among a North Indian population
|
Rana, Garima
|
|
2017
|
9 |
1 |
p. 51-55
|
artikel
|
| 2 |
Behavioural changes, sharing behaviour and psychological responses after receiving direct-to-consumer genetic test results: a systematic review and meta-analysis
|
Stewart, Kelly F. J.
|
|
2017
|
9 |
1 |
p. 1-18
|
artikel
|
| 3 |
Consumer attitudes towards the establishment of a national Australian familial cancer research database by the Inherited Cancer Connect (ICCon) Partnership
|
Forrest, Laura
|
|
2017
|
9 |
1 |
p. 57-64
|
artikel
|
| 4 |
Diagnosis of rare diseases under focus: impacts for Canadian patients
|
Esquivel-Sada, Daphne
|
|
2017
|
9 |
1 |
p. 37-50
|
artikel
|
| 5 |
Exploring approaches to facilitate family communication of genetic risk information after cystic fibrosis population carrier screening
|
Gorrie, Anita
|
|
2017
|
9 |
1 |
p. 71-80
|
artikel
|
| 6 |
Exploring Asian Indian and Pakistani views about cancer and participation in cancer genetics research: toward the development of a community genetics intervention
|
Leader, Amy E.
|
|
2017
|
9 |
1 |
p. 27-35
|
artikel
|
| 7 |
Great expectations: patient perspectives and anticipated utility of non-diagnostic genomic-sequencing results
|
Hylind, Robyn
|
|
2017
|
9 |
1 |
p. 19-26
|
artikel
|
| 8 |
Life paths of patients with transthyretin-related familial amyloid polyneuropathy Val30Met: a descriptive study
|
Lopes, Alice
|
|
2017
|
9 |
1 |
p. 93-99
|
artikel
|
| 9 |
Preferences for multigene panel testing for hereditary breast cancer risk among ethnically diverse BRCA-uninformative families
|
Vicuña, Belinda
|
|
2017
|
9 |
1 |
p. 81-92
|
artikel
|
| 10 |
The clinical and genetic Spectrum of Maroteaux-Lamy syndrome (Mucopolysaccharidosis VI) in the Eastern Province of Saudi Arabia
|
Al-Sannaa, Nouriya Abbas
|
|
2017
|
9 |
1 |
p. 65-70
|
artikel
|
| 11 |
The M2 haplotype of ANXA5 gene in the context of unexplained recurrent miscarriages
|
Markoff, Arseni
|
|
2017
|
9 |
1 |
p. 101-102
|
artikel
|
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