| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Components of genetic counsellor education: A systematic review of the peer-reviewed literature
|
Ingvoldstad, C.
|
|
2015
|
7 |
2 |
p. 107-118
|
artikel
|
| 2 |
Consenting postpartum women for use of routinely collected biospecimens and/or future biospecimen collection
|
Kozinetz, Claudia A.
|
|
2016
|
7 |
2 |
p. 153-158
|
artikel
|
| 3 |
Health research: working with Indigenous People in Peru
|
Zavaleta, Carol
|
|
2016
|
7 |
2 |
p. 173-174
|
artikel
|
| 4 |
“It gives them more options”: preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcare
|
Archibald, Alison D.
|
|
2016
|
7 |
2 |
p. 159-171
|
artikel
|
| 5 |
Participant views on consent in cancer genetics research: preparing for the precision medicine era
|
Edwards, Karen L.
|
|
2016
|
7 |
2 |
p. 133-143
|
artikel
|
| 6 |
Prevention of sickle cell disease: observations on females with the sickle cell trait from the Manchester project, Jamaica
|
Mason, Karlene
|
|
2015
|
7 |
2 |
p. 127-132
|
artikel
|
| 7 |
Relevant ethical consideration in research with indigenous people in Peru
|
Minaya, Gabriela
|
|
2016
|
7 |
2 |
p. 175-176
|
artikel
|
| 8 |
Was it worth it? Patients’ perspectives on the perceived value of genomic-based individualized medicine
|
Halverson, Colin ME
|
|
2016
|
7 |
2 |
p. 145-152
|
artikel
|
| 9 |
Wide disparity of clinical genetics services and EU rare disease research funding across Europe
|
Lynch, Sally Ann
|
|
2015
|
7 |
2 |
p. 119-126
|
artikel
|
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