| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A feasible molecular diagnostic strategy for rare genetic disorders within resource-constrained environments
|
Mudau, Maria Mabyalwa
|
|
|
15 |
1 |
p. 39-48
|
artikel
|
| 2 |
Ethics of artificial intelligence in prenatal and pediatric genomic medicine
|
Coghlan, Simon
|
|
|
15 |
1 |
p. 13-24
|
artikel
|
| 3 |
Growth in perceived clinical genetics competency among primary care providers participating in genomic population health screening
|
Hansen, Christina A.
|
|
|
15 |
1 |
p. 33-37
|
artikel
|
| 4 |
Healthcare and support experiences of adolescents and young adults diagnosed with 47,XXY, 47,XXX, and 48,XXYY
|
Ahlawat, Nivedita
|
|
|
15 |
1 |
p. 75-83
|
artikel
|
| 5 |
Latina immigrants’ breast and colon cancer causal attributions: genetics is key
|
Fiallos, Katie
|
|
|
15 |
1 |
p. 59-73
|
artikel
|
| 6 |
Receiving de novo genetic diagnoses for autism with intellectual disability: parents’ views of impacts on families’ reproductive decisions
|
Klitzman, Robert
|
|
|
15 |
1 |
p. 85-96
|
artikel
|
| 7 |
Retrospective chart analysis to determine the impact of a patient-facing digital risk stratification tool combined with a clinical screener for hereditary cancer genetic risk assessment triage in a community oncology clinic
|
Shane-Carson, Kate P.
|
|
|
15 |
1 |
p. 25-31
|
artikel
|
| 8 |
Short Communication: Lived experience perspectives on genetic testing for a rare eye disease
|
Tam, Mallorie T.
|
|
|
15 |
1 |
p. 97-101
|
artikel
|
| 9 |
Survey of attitude to human genome modification in Nigeria
|
Jibrilla, Maryam
|
|
|
15 |
1 |
p. 1-11
|
artikel
|
| 10 |
“There should be one spot that you can go:” BRCA mutation carriers’ perspectives on cancer risk management and a hereditary cancer registry
|
Hynes, J.
|
|
|
15 |
1 |
p. 49-58
|
artikel
|
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