nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
An integrative review of factors that influence reproductive decisions in women with sickle cell disease
|
Rance, Josephine Claire |
|
2018 |
10 |
2 |
p. 161-169 |
artikel |
2 |
“A perfect society”— Swedish policymakers’ ethical and social views on preconception expanded carrier screening
|
Matar, Amal |
|
2018 |
10 |
2 |
p. 267-280 |
artikel |
3 |
Barriers to the identification of familial hypercholesterolemia among primary care providers
|
Zimmerman, John |
|
2018 |
10 |
2 |
p. 229-236 |
artikel |
4 |
Correction to: 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 |
10 |
2 |
p. 321 |
artikel |
5 |
Correction to: EUROCAT: an update on its functions and activities
|
Tucker, F. D. |
|
2018 |
10 |
2 |
p. 323 |
artikel |
6 |
Direct-to-consumer carrier screening for cystic fibrosis via a hospital website: a 6-year evaluation
|
Holtkamp, Kim C. A. |
|
2018 |
10 |
2 |
p. 249-257 |
artikel |
7 |
Disclosure of diagnosis to at-risk relatives by individuals diagnosed with hypertrophic cardiomyopathy (HCM)
|
Hudson, Janella |
|
2018 |
10 |
2 |
p. 207-217 |
artikel |
8 |
Experiences of patients seeking to participate in variant of uncertain significance reclassification research
|
Makhnoon, Sukh |
|
2018 |
10 |
2 |
p. 189-196 |
artikel |
9 |
Exploring the perceived self-efficacy of genetic counselors as teachers
|
Gasparini, Justin |
|
2018 |
10 |
2 |
p. 313-319 |
artikel |
10 |
Family health history and genetic services—the East Baltimore community stakeholder interview project
|
Sanghavi, Kunal |
|
2018 |
10 |
2 |
p. 219-227 |
artikel |
11 |
Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome
|
Henriksson, Isabelle |
|
2018 |
10 |
2 |
p. 259-266 |
artikel |
12 |
High-risk women’s risk perception after receiving personalized polygenic breast cancer risk information
|
Forrest, Laura Elenor |
|
2018 |
10 |
2 |
p. 197-206 |
artikel |
13 |
Information exchange between patients with Lynch syndrome and their genetic and non-genetic health professionals: whose responsibility?
|
Douma, Kirsten F. L. |
|
2018 |
10 |
2 |
p. 237-247 |
artikel |
14 |
Risk perception and screening behavior of Filipino women at risk for breast cancer: implications for cancer genetic counseling
|
Lagarde, John Benedict B. |
|
2018 |
10 |
2 |
p. 281-289 |
artikel |
15 |
“This could be me”: exploring the impact of genetic risk for Huntington’s disease young caregivers
|
Dondanville, Danielle S. |
|
2018 |
10 |
2 |
p. 291-302 |
artikel |
16 |
Uncertainty related to multigene panel testing for cancer: a qualitative study on counsellors’ and counselees’ views
|
Medendorp, Niki M. |
|
2018 |
10 |
2 |
p. 303-312 |
artikel |
17 |
What do people think about genetics? A systematic review
|
LePoire, Erin |
|
2018 |
10 |
2 |
p. 171-187 |
artikel |