| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A comparison of cancer risk assessment and testing outcomes in patients from underserved vs. tertiary care settings
|
Rana, Huma Q.
|
|
2017
|
9 |
3 |
p. 233-241
|
artikel
|
| 2 |
An Internet support group for parents of children with neurofibromatosis type 1: a qualitative analysis
|
Martin, Staci
|
|
2018
|
9 |
3 |
p. 327-334
|
artikel
|
| 3 |
Cancer genetic counseling communication with low-income Chinese immigrants
|
Cheng, Janice Ka Yan
|
|
2017
|
9 |
3 |
p. 263-276
|
artikel
|
| 4 |
Experience of Asian males communicating cardiac genetic risk within the family
|
Kam, Sylvia
|
|
2018
|
9 |
3 |
p. 293-303
|
artikel
|
| 5 |
From the laboratory to the clinic: sharing BRCA VUS reclassification tools with practicing genetics professionals
|
Augusto, Bianca M.
|
|
2017
|
9 |
3 |
p. 209-215
|
artikel
|
| 6 |
Germline mutations in BRCA1 and BRCA2 incidentally revealed in a biobank research study: experiences from re-contacting mutation carriers and relatives
|
Nilsson, Martin P.
|
|
2017
|
9 |
3 |
p. 201-208
|
artikel
|
| 7 |
“I would like to discuss it further with an expert”: a focus group study of Finnish adults’ perspectives on genetic secondary findings
|
Vornanen, M.
|
|
2018
|
9 |
3 |
p. 305-314
|
artikel
|
| 8 |
Mainstreaming genetics in palliative care: barriers and suggestions for clinical genetic services
|
Dearing, A.
|
|
2017
|
9 |
3 |
p. 243-256
|
artikel
|
| 9 |
Patient and provider perspectives on the development of personalized medicine: a mixed-methods approach
|
Puryear, Lauren
|
|
2017
|
9 |
3 |
p. 283-291
|
artikel
|
| 10 |
Predictors of adverse psychological experiences surrounding genome-wide profiling for disease risk
|
Broady, K. M.
|
|
2017
|
9 |
3 |
p. 217-225
|
artikel
|
| 11 |
Reproductive decision making: interviews with mothers of children with undiagnosed developmental delay
|
Pond, Emily
|
|
2018
|
9 |
3 |
p. 315-325
|
artikel
|
| 12 |
Risk stratification, genomic data and the law
|
Hall, Alison
|
|
2018
|
9 |
3 |
p. 195-199
|
artikel
|
| 13 |
Thalassemia: a prevalent disease yet unknown term among college students in Saudi Arabia
|
Olwi, Duaa Ibrahim
|
|
2017
|
9 |
3 |
p. 277-282
|
artikel
|
| 14 |
The accessibility and utilization of genetic testing for inherited heart rhythm disorders: a Canadian cross-sectional survey study
|
Roston, Thomas M.
|
|
2017
|
9 |
3 |
p. 257-262
|
artikel
|
| 15 |
The effect of parental age on NF1 patients in Turkey
|
Sharafi, P.
|
|
2017
|
9 |
3 |
p. 227-232
|
artikel
|
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