| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A rare disorder or not? How a child with jaundice changed a nationwide regimen in the Netherlands
|
Heuvel, E. A. L. van den
|
|
2017
|
8 |
4 |
p. 335-339
|
artikel
|
| 2 |
Blame—a novel by Tony Holtzman
|
Cornel, Martina C.
|
|
2017
|
8 |
4 |
p. 253-254
|
artikel
|
| 3 |
Diversity and inclusion in genomic research: why the uneven progress?
|
Bentley, Amy R.
|
|
2017
|
8 |
4 |
p. 255-266
|
artikel
|
| 4 |
Focusing attention on ancestral diversity within genomics research: a potential means for promoting equity in the provision of genomics based healthcare services in developing countries
|
Sirisena, Nirmala D.
|
|
2017
|
8 |
4 |
p. 275-281
|
artikel
|
| 5 |
Genetics in an isolated population like Finland: a different basis for genomic medicine?
|
Kääriäinen, Helena
|
|
2017
|
8 |
4 |
p. 319-326
|
artikel
|
| 6 |
Genomics for all in the 21st century?
|
Cornel, Martina C.
|
|
2017
|
8 |
4 |
p. 249-251
|
artikel
|
| 7 |
Inclusion of diverse populations in genomic research and health services: Genomix workshop report
|
Mathew, Savio S.
|
|
2017
|
8 |
4 |
p. 267-273
|
artikel
|
| 8 |
Increasing the involvement of diverse populations in genomics-based health care—lessons from haemoglobinopathies
|
Robinson, Helen M.
|
|
2017
|
8 |
4 |
p. 311-318
|
artikel
|
| 9 |
Leveraging community-based participatory research capacity to recruit Pacific Islanders into a genetics study
|
McElfish, Pearl A.
|
|
2017
|
8 |
4 |
p. 283-291
|
artikel
|
| 10 |
Racial minority group interest in direct-to-consumer genetic testing: findings from the PGen study
|
Landry, Latrice
|
|
2017
|
8 |
4 |
p. 293-301
|
artikel
|
| 11 |
Referral to cancer genetic counseling: do migrant status and patients’ educational background matter?
|
Giessen, J. A. M. van der
|
|
2017
|
8 |
4 |
p. 303-310
|
artikel
|
| 12 |
With expanded carrier screening, founder populations run the risk of being overlooked
|
Mathijssen, Inge B.
|
|
2017
|
8 |
4 |
p. 327-333
|
artikel
|
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