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                             20 gevonden resultaten
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
                             20 gevonden resultaten
 
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