| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A review of key terminology and definitions used for birth defects globally
|
Malherbe, HL
|
|
|
14 |
3 |
p. 241-262
|
artikel
|
| 2 |
Co-designing interventions to ‘live well’: experiences and perceptions of the Genetic, Undiagnosed and Rare Disease (GUaRD) community
|
Beadell, Inez
|
|
|
14 |
3 |
p. 295-305
|
artikel
|
| 3 |
Digital interventions for genomics and genetics education, empowerment, and service engagement: A systematic review
|
Gasteiger, Norina
|
|
|
14 |
3 |
p. 227-240
|
artikel
|
| 4 |
Evaluating cancer genetic services in a safety net system: overcoming barriers for a lasting impact beyond the CHARM research project
|
Okuyama, Sonia
|
|
|
14 |
3 |
p. 329-336
|
artikel
|
| 5 |
Exploring the impact of the reclassification of a hereditary cancer syndrome gene variant: emerging themes from a qualitative study
|
Wedd, Laura
|
|
|
14 |
3 |
p. 307-317
|
artikel
|
| 6 |
Fundamental knowledge taught in compulsory education for effective genetic counseling: a qualitative study of descriptions in textbooks
|
Sakai, Eri
|
|
|
14 |
3 |
p. 263-274
|
artikel
|
| 7 |
Knowledge, attitude, and perceptions about cancer genetic testing in clinical practice in Karachi, Pakistan
|
Shafqat, Shameel
|
|
|
14 |
3 |
p. 337-344
|
artikel
|
| 8 |
Never “totally prepared”: Support groups on helping families prepare for a child with a genetic condition
|
Craig, Kaitlynn P.
|
|
|
14 |
3 |
p. 319-327
|
artikel
|
| 9 |
Pakistani healthcare professionals’ perceptions of communication with patients and their relatives about hereditary breast cancer: a qualitative study in a LMIC
|
Ahmed, Shenaz
|
|
|
14 |
3 |
p. 287-294
|
artikel
|
| 10 |
Public’s awareness of biobanks and willingness to participate in biobanking: the moderating role of social value orientation
|
Grežo, Matúš
|
|
|
14 |
3 |
p. 275-285
|
artikel
|
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