| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acceptability of dried blood spot collection by primary caregivers of Filipino patients with maple syrup urine disease (MSUD) and phenylketonuria (PKU)
|
Merencilla, Roxanne Janica E.
|
|
|
15 |
6 |
p. 699-710
|
artikel
|
| 2 |
Deciphering the needs of patients with hereditary breast and ovarian Cancer in the Process of Genetic Counseling to Inform the Development of a Mobile Support App: a qualitative study in Germany
|
Ammon, Nils
|
|
|
15 |
6 |
p. 603-613
|
artikel
|
| 3 |
Do not overlook the possibility of genome-edited somatic cells ending up in the human germline
|
Chin, Alexis Heng Boon
|
|
|
15 |
6 |
p. 749-752
|
artikel
|
| 4 |
Engaging communities: A scoping literature review of community-based participatory research in genetics service delivery settings
|
Zierhut, Heather A.
|
|
|
15 |
6 |
p. 583-602
|
artikel
|
| 5 |
Factors influencing pregnant women’s decision to accept or decline prenatal screening and diagnosis – a qualitative study
|
Ternby, Ellen
|
|
|
15 |
6 |
p. 711-721
|
artikel
|
| 6 |
Feasibility of an environmental scan–based approach to collecting information about factors impacting cancer genetics services in Latin American countries
|
Bednar, Erica M.
|
|
|
15 |
6 |
p. 681-686
|
artikel
|
| 7 |
Genetic testing perspectives in Pakistani population: a survey on knowledge, attitudes, awareness, and concerns
|
Uzair, Mohammad
|
|
|
15 |
6 |
p. 631-640
|
artikel
|
| 8 |
How to communicate and what to disclose to participants in a recall-by-genotype research approach: a multistep empirical study
|
Tschigg, Katharina
|
|
|
15 |
6 |
p. 615-630
|
artikel
|
| 9 |
Key challenges in developing a gene therapy for Usher syndrome: machine-assisted scoping review
|
Bhat, Rajeshwari
|
|
|
15 |
6 |
p. 735-747
|
artikel
|
| 10 |
Key contextual factors involved with participation in medical and genomic screening and research for African American and White Americans: a qualitative inquiry
|
Smith, Crystal Lederhos
|
|
|
15 |
6 |
p. 723-733
|
artikel
|
| 11 |
Knowledge, attitude and acceptance regarding bone marrow transplantation in caregivers of beta-thalassemia major patients
|
Jayaram, Purva Reddy
|
|
|
15 |
6 |
p. 673-679
|
artikel
|
| 12 |
Negative results from DNA-based population screening for adult-onset diseases: the recipients’ experience
|
Russo, Felicia
|
|
|
15 |
6 |
p. 653-664
|
artikel
|
| 13 |
Opportunities and challenges for identifying undiagnosed Rare Disease patients through analysis of primary care records: long QT syndrome as a test case
|
Evans, William
|
|
|
15 |
6 |
p. 687-698
|
artikel
|
| 14 |
Sickle cell disease awareness and perception among Christian religious leaders in Accra Metropolis: a qualitative study
|
Okyere, Rebecca
|
|
|
15 |
6 |
p. 641-652
|
artikel
|
| 15 |
Spinal muscular atrophy carrier screening program: awareness and attitude of healthcare professionals in Turkey
|
Celik, Kubra Muge
|
|
|
15 |
6 |
p. 665-672
|
artikel
|
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