| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A collaborative genetic carrier screening model for the British Ashkenazi Jewish community
|
Ziff, Monica
|
|
|
13 |
1 |
p. 133-135
|
artikel
|
| 2 |
A systematic review of the views of healthcare professionals on the scope of preimplantation genetic testing
|
Siermann, Maria
|
|
|
13 |
1 |
p. 1-11
|
artikel
|
| 3 |
Comprehension of skin cancer genetic risk feedback in primary care patients
|
Khan, Erva
|
|
|
13 |
1 |
p. 113-119
|
artikel
|
| 4 |
Correction to: Treatment decision‑making in sickle cell disease patients
|
Booth, A.
|
|
|
13 |
1 |
p. 153-154
|
artikel
|
| 5 |
Development and pilot testing of an online decision aid for women considering risk-stratified breast screening
|
Lippey, Jocelyn
|
|
|
13 |
1 |
p. 137-141
|
artikel
|
| 6 |
Evaluating the model of offering expanded genetic carrier screening to high school students within the Sydney Jewish community
|
Barlow-Stewart, Kristine
|
|
|
13 |
1 |
p. 121-131
|
artikel
|
| 7 |
Extended family thalassemia screening as a feasible alternative method to be implemented in identifying carriers in West Java, Indonesia
|
Susanah, Susi
|
|
|
13 |
1 |
p. 103-112
|
artikel
|
| 8 |
Fragmented responsibility: views of Israeli HCPs regarding patient recontact following variant reclassification
|
Fridman, Alma Levin
|
|
|
13 |
1 |
p. 13-18
|
artikel
|
| 9 |
Hereditary cancer panel testing challenges and solutions for the latinx community: costs, access, and variants
|
Douglas, Michael P.
|
|
|
13 |
1 |
p. 75-80
|
artikel
|
| 10 |
IMPACT webinars: Improving Patient Access to genetic Counselling and Testing using webinars—the Alberta experience with hypertrophic cardiomyopathy
|
Christian, Susan
|
|
|
13 |
1 |
p. 81-89
|
artikel
|
| 11 |
Parents’ perspectives, experiences, and need for support when communicating with their children about the psychiatric manifestations of 22q11.2 deletion syndrome (22q11DS)
|
Cook, Courtney B.
|
|
|
13 |
1 |
p. 91-101
|
artikel
|
| 12 |
“Right diet for the right person”: a focus group study of nutritionist-dietitians’ perspectives on nutritional genomics and gene-based nutrition advice
|
Nacis, Jacus S.
|
|
|
13 |
1 |
p. 49-57
|
artikel
|
| 13 |
Stakeholder attitudes towards establishing a national genomics registry of inherited cancer predisposition: a qualitative study
|
Meiser, Bettina
|
|
|
13 |
1 |
p. 59-73
|
artikel
|
| 14 |
Transgender and gender-diverse (TGD) individuals’ perspectives on research seeking genetic variants associated with TGD identities: a qualitative study
|
Rajkovic, Antoine
|
|
|
13 |
1 |
p. 31-48
|
artikel
|
| 15 |
Treatment decision-making in sickle cell disease patients
|
Booth, A.
|
|
|
13 |
1 |
p. 143-151
|
artikel
|
| 16 |
When guidelines face reality — Lynch syndrome screening in the setting of public health system in a developing country
|
Kozak, Vanessa Nascimento
|
|
|
13 |
1 |
p. 19-29
|
artikel
|
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