| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A content analysis of direct-to-consumer DNA testing on TikTok
|
Basch, Corey H.
|
|
|
12 |
3 |
p. 489-492
|
artikel
|
| 2 |
Barriers and strategies to integrate medical genetics and primary care in underserved populations: a scoping review
|
Chou, Ann F.
|
|
|
12 |
3 |
p. 291-309
|
artikel
|
| 3 |
Baseline knowledge and receptiveness to genetic testing for hereditary breast and ovarian cancer syndromes in Chinese high-risk females
|
Chu, Annie Tsz-Wai
|
|
|
12 |
3 |
p. 431-438
|
artikel
|
| 4 |
Birth prevalence of congenital anomalies in Argentina, according to socioeconomic level
|
Bronberg, Ruben
|
|
|
12 |
3 |
p. 345-355
|
artikel
|
| 5 |
Clinical and community genetics services in the Dutch Caribbean
|
Verberne, Eline A.
|
|
|
12 |
3 |
p. 497-501
|
artikel
|
| 6 |
Correction to: Geographic distribution of live births and infant mortality from congenital anomalies in Brazil, 2012–2017
|
Reis, Luzivan Costa
|
|
|
12 |
3 |
p. 387
|
artikel
|
| 7 |
Disclosure of familial implications of pathogenic variants in breast-cancer genes to patients: Opportunity for prompting family communication
|
Makhnoon, Sukh
|
|
|
12 |
3 |
p. 439-447
|
artikel
|
| 8 |
Geographic distribution of live births and infant mortality from congenital anomalies in Brazil, 2012–2017
|
Reis, Luzivan Costa
|
|
|
12 |
3 |
p. 377-386
|
artikel
|
| 9 |
Healthcare providers attitudes towards risk stratification of adopted patients with limited family history information: a cross-sectional survey
|
Saltzman, Barbara
|
|
|
12 |
3 |
p. 485-488
|
artikel
|
| 10 |
Hereditary diseases and child wish: exploring motives, considerations, and the (joint) decision-making process of genetically at-risk couples
|
Severijns, Y.
|
|
|
12 |
3 |
p. 325-335
|
artikel
|
| 11 |
Interpretation and management of genetic test results by Canadian family physicians: a multiple choice survey of performance
|
Skinner, Stephanie J.
|
|
|
12 |
3 |
p. 479-484
|
artikel
|
| 12 |
Knowledge and perceptions of BRCA1/2 genetic testing and needs of diverse women with a personal or family history of breast cancer in South Florida
|
Jones, Tarsha
|
|
|
12 |
3 |
p. 415-429
|
artikel
|
| 13 |
Modelled epidemiological data for selected congenital disorders in South Africa
|
Malherbe, Helen L.
|
|
|
12 |
3 |
p. 357-376
|
artikel
|
| 14 |
Modernizing family health history: achievable strategies to reduce implementation gaps
|
Wildin, Robert S.
|
|
|
12 |
3 |
p. 493-496
|
artikel
|
| 15 |
Neonatal screening program for five conditions in Honduras
|
Buckley, Michelle Melissa Miralda
|
|
|
12 |
3 |
p. 389-395
|
artikel
|
| 16 |
Oncologists’ perspectives of telephone genetic counseling to facilitate germline BRCA1/2 testing for their patients with high-grade serous ovarian cancer
|
Hemming, Pierre
|
|
|
12 |
3 |
p. 449-457
|
artikel
|
| 17 |
Preconception expanded carrier screening: a focus group study with relatives of mucopolysaccharidosis type III patients and the general population
|
Conijn, Thirsa
|
|
|
12 |
3 |
p. 311-323
|
artikel
|
| 18 |
Public attitudes towards the genetic testing in Georgia
|
Kvaratskhelia, Eka
|
|
|
12 |
3 |
p. 407-414
|
artikel
|
| 19 |
Recruiting for diversity: a pilot test of recruitment strategies for a national alcohol survey with mail-in genetic data collection
|
Chartier, Karen G.
|
|
|
12 |
3 |
p. 459-468
|
artikel
|
| 20 |
Role of older generations in the family’s adjustment to Huntington disease
|
Oliveira, Carla Roma
|
|
|
12 |
3 |
p. 469-477
|
artikel
|
| 21 |
Students’ attitudes towards somatic genome editing versus genome editing of the germline using an example of familial leukemia
|
Vajen, Beate
|
|
|
12 |
3 |
p. 397-406
|
artikel
|
| 22 |
Undiagnosed haemoglobinopathies among pregnant women attending antenatal care clinics in Pune, India
|
Dharmarajan, Sumedha
|
|
|
12 |
3 |
p. 337-344
|
artikel
|
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