| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Caregiver-reported barriers to care for children and adults with Williams Syndrome
|
Barnhardt, Elizabeth W.
|
|
|
15 |
4 |
p. 375-386
|
artikel
|
| 2 |
Congenital anomalies in Santa Catarina, Southern Brazil: macroregional and temporal birth prevalence for the period 2011–2020
|
Krieck, Laysa Kariny
|
|
|
15 |
4 |
p. 423-431
|
artikel
|
| 3 |
Exploring family communication preferences in hereditary breast and ovarian cancer and Lynch syndrome: a national Canadian survey
|
Burke, Kimberly
|
|
|
15 |
4 |
p. 387-400
|
artikel
|
| 4 |
Family communication of cancer genetic test results in an ethnically diverse population: a qualitative exploration of more than 200 patients
|
Hodan, Rachel
|
|
|
15 |
4 |
p. 363-374
|
artikel
|
| 5 |
Health-related roles of older generations in families with inherited genetic conditions: a scoping review
|
Oliveira, Carla Roma
|
|
|
15 |
4 |
p. 351-361
|
artikel
|
| 6 |
Is Tunisia ready for precision medicine? Challenges of medical genomics within a LMIC healthcare system
|
Trabelsi, Narjes
|
|
|
15 |
4 |
p. 339-350
|
artikel
|
| 7 |
Knowledge of genetics and attitudes toward genetic testing among university students in Indonesia
|
Hermanto, Iskandar
|
|
|
15 |
4 |
p. 433-447
|
artikel
|
| 8 |
“Living with a question mark”: psychosocial experience of Portuguese young adults at risk for hereditary amyloid transthyretin amyloidosis with polyneuropathy
|
Pereira, José D.
|
|
|
15 |
4 |
p. 401-411
|
artikel
|
| 9 |
Prevalence of congenital anomalies and prenatal diagnosis by birth institution (public vs. non-public): indicators of inequality in access to elective termination of pregnancy for fetal anomalies
|
Brun, Paloma
|
|
|
15 |
4 |
p. 413-422
|
artikel
|
| 10 |
“Unnatural resources?”: parallels and distinctions between the Newfoundland Genome and traditional resource sectors
|
Skeard, Janelle
|
|
|
15 |
4 |
p. 449-459
|
artikel
|
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