| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
African American mothers’ attitudes towards genetic testing in the InterGEN study
|
Wright, Michelle L.
|
|
|
11 |
3 |
p. 285-290
|
artikel
|
| 2 |
A large family with CYLD cutaneous syndrome: medical genetics at the community level
|
Arruda, Anderson Pontes
|
|
|
11 |
3 |
p. 279-284
|
artikel
|
| 3 |
Applying Rogers’ framework to evaluate public awareness and knowledge of medical genetics in a developing country
|
Asadollahi, Hamid
|
|
|
11 |
3 |
p. 367-375
|
artikel
|
| 4 |
Birth prevalence of congenital anomalies in the City of Buenos Aires, Argentina, according to socioeconomic level
|
Bronberg, Ruben
|
|
|
11 |
3 |
p. 303-311
|
artikel
|
| 5 |
Characteristics predicting recommendation for familial breast cancer referral in a cohort of women from primary care
|
Lee, Siang Ing
|
|
|
11 |
3 |
p. 331-338
|
artikel
|
| 6 |
Empowering newborn screening programs in African countries through establishment of an international collaborative effort
|
Therrell, Bradford L.
|
|
|
11 |
3 |
p. 253-268
|
artikel
|
| 7 |
Gene editing and disabled people: a response to Felicity Boardman
|
de Miguel Beriain, Iñigo
|
|
|
11 |
3 |
p. 241-243
|
artikel
|
| 8 |
How genomic information is accessed in clinical practice: an electronic survey of UK general practitioners
|
Evans, W. R. H.
|
|
|
11 |
3 |
p. 377-386
|
artikel
|
| 9 |
Letter to the editor. Gene editing and disabled people: a response to Iñigo de Miguel Beriain
|
Boardman, Felicity
|
|
|
11 |
3 |
p. 245-247
|
artikel
|
| 10 |
Letter to the Editor: Time to update the language of genetics from the nineteenth to the twenty-first century: a response to Schmidtke and Cornel
|
Small, Neil
|
|
|
11 |
3 |
p. 249-251
|
artikel
|
| 11 |
Online BRCA1/2 screening in the Australian Jewish community: a qualitative study
|
Yuen, Jeanette
|
|
|
11 |
3 |
p. 291-302
|
artikel
|
| 12 |
Parent and child perspectives on family interactions related to melanoma risk and prevention after CDKN2A/p16 testing of minor children
|
Wu, Yelena P.
|
|
|
11 |
3 |
p. 321-329
|
artikel
|
| 13 |
Prenatal detection of congenital anomalies and related factors in Argentina
|
Bidondo, Maria Paz
|
|
|
11 |
3 |
p. 313-320
|
artikel
|
| 14 |
Prevalence of mutations in a diverse cohort of 3162 women tested via the same multigene cancer panel in a managed care health plan
|
Alvarado, Mónica
|
|
|
11 |
3 |
p. 359-366
|
artikel
|
| 15 |
Primary care physician experiences utilizing a family health history tool with electronic health record–integrated clinical decision support: an implementation process assessment
|
Lemke, Amy A.
|
|
|
11 |
3 |
p. 339-350
|
artikel
|
| 16 |
Quality of life and comprehensive health supervision for children with Down syndrome in Thailand
|
Rojnueangnit, Kitiwan
|
|
|
11 |
3 |
p. 351-358
|
artikel
|
| 17 |
The implementation of pharmacogenomics into UK general practice: a qualitative study exploring barriers, challenges and opportunities
|
Rafi, I.
|
|
|
11 |
3 |
p. 269-277
|
artikel
|
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