| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Attitudes among South African university staff and students towards disclosing secondary genetic findings
|
Spies, Georgina
|
|
|
12 |
1 |
p. 171-184
|
artikel
|
| 2 |
Attitudes and impact among people with abnormal premarital screening test results in Muscat governorate’s primary healthcare centers in 2018
|
Al Zeedi, Manar Al Sanaa Ali
|
|
|
12 |
1 |
p. 163-169
|
artikel
|
| 3 |
Birth defect mortality in India 1990–2017: estimates from the Global Burden of Disease data
|
Ujagare, Dhammasagar
|
|
|
12 |
1 |
p. 81-90
|
artikel
|
| 4 |
Communication about breast cancer genetic counseling with patients with limited health literacy or a migrant background: evaluation of a training program for healthcare professionals
|
van der Giessen, Jeanine
|
|
|
12 |
1 |
p. 91-99
|
artikel
|
| 5 |
Dying to see you? Deaths on a clinical genetics waiting list in the Republic of Ireland; what are the consequences?
|
Bradley, Lisa
|
|
|
12 |
1 |
p. 121-127
|
artikel
|
| 6 |
Electronic informed consent information for residual newborn specimen research: findings from focus groups with diverse populations
|
Frost, Caren J.
|
|
|
12 |
1 |
p. 199-203
|
artikel
|
| 7 |
Feasibility of establishing a network of community health workers to support care of people with sickle cell disease in Kumasi, Ghana
|
Buser, Julie M.
|
|
|
12 |
1 |
p. 155-161
|
artikel
|
| 8 |
Genetic epidemiology of hemoglobinopathies among Iraqi Kurds
|
Al-Allawi, Nasir
|
|
|
12 |
1 |
p. 5-14
|
artikel
|
| 9 |
Hmong participants’ reactions to return of individual and community pharmacogenetic research results: “A positive light for our community”
|
Holzer, K.
|
|
|
12 |
1 |
p. 53-65
|
artikel
|
| 10 |
Impacts of personal DNA ancestry testing
|
Rubanovich, Caryn Kseniya
|
|
|
12 |
1 |
p. 37-52
|
artikel
|
| 11 |
Increased ease of access to genetic counseling for low-income women with breast cancer using a point of care screening tool
|
Rao, Smita K.
|
|
|
12 |
1 |
p. 129-136
|
artikel
|
| 12 |
Influence of gender norms in relation to child’s quality of care: follow-up of families of children with SCD identified through NBS in Tanzania
|
Bukini, Daima
|
|
|
12 |
1 |
p. 143-154
|
artikel
|
| 13 |
In memoriam Prof. Dr. Leo P. ten Kate
|
Cornel, Martina C.
|
|
|
12 |
1 |
p. 1-3
|
artikel
|
| 14 |
Knowing, relationships and trust—citizens’ perceptions of whole genome sequencing for the Genetics Clinic of the Future
|
Schumann, Simone
|
|
|
12 |
1 |
p. 67-80
|
artikel
|
| 15 |
Patients’ decision to contribute to a biobank in the light of the patient-recruiter relationship—a qualitative study of broad consent in a hospital setting
|
Bosisio, Francesca
|
|
|
12 |
1 |
p. 15-25
|
artikel
|
| 16 |
Public engagement with genomic medicine: a summary of town hall discussions
|
Etchegary, Holly
|
|
|
12 |
1 |
p. 27-35
|
artikel
|
| 17 |
Reproductive decision-making in the context of hereditary cancer: the effects of an online decision aid on informed decision-making
|
Reumkens, Kelly
|
|
|
12 |
1 |
p. 101-110
|
artikel
|
| 18 |
Sickle cell trait newborn screen results: disclosure and management
|
Lilley, Margaret
|
|
|
12 |
1 |
p. 137-142
|
artikel
|
| 19 |
Specialist recommendation for chemoprevention medications in patients at familial risk of breast cancer: a cross-sectional survey in England
|
Lee, Siang Ing
|
|
|
12 |
1 |
p. 111-120
|
artikel
|
| 20 |
The impact of insurance on equitable access to non-invasive prenatal screening (NIPT): private insurance may not pay
|
Benoy, Megan E.
|
|
|
12 |
1 |
p. 185-197
|
artikel
|
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