Detalhe da pesquisa
1.
Exploring genetic counselors' experiences with non-paternity in clinical settings.
J Genet Couns
; 2024 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38323428
2.
Adolescents' implicit and explicit attitudes toward their peers with genetic conditions.
J Adolesc
; 2024 May 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38711256
3.
Considerations for the use of qualitative methodologies in genetic counseling research.
J Genet Couns
; 32(2): 300-314, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36271905
4.
Genetic counselors' research dissemination practices and attitudes.
J Genet Couns
; 2023 Jun 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37382025
5.
The experiences of adolescent siblings of children with rare genetic conditions: "It's made me who I am".
J Genet Couns
; 32(1): 224-234, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36123145
6.
A novel online genomic counseling and variant interpretation certificate: Learning design, learning analytics, and evaluation.
J Genet Couns
; 32(6): 1280-1287, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37424058
7.
Implementing genomics in the neonatal period: An assessment of parental decision making and anxiety.
J Genet Couns
; 31(6): 1306-1316, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35733279
8.
Review of 10 years of preimplantation genetic diagnosis in South Africa: implications for a low-to-middle-income country.
J Assist Reprod Genet
; 36(9): 1909-1916, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31350724
9.
Promoting methodological integrity in qualitative genetic counseling research: Insights arising from the commentary by Lynch, Gillam, and Vears.
J Genet Couns
; 2023 Nov 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37937670
10.
Experiences With Genetic Counseling, Testing, and Diagnosis Among Adolescents With a Genetic Condition: A Scoping Review.
JAMA Pediatr
; 176(2): 185-195, 2022 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34807246
11.
Far and wide: Exploring provider utilization of remote service provision for genome-wide sequencing in Canada.
Mol Genet Genomic Med
; 9(10): e1784, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34532994
12.
Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia.
Fam Cancer
; 16(3): 441-446, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28185119
13.
Breast cancer in high-risk Afrikaner families: Is BRCA founder mutation testing sufficient?
S Afr Med J
; 106(3): 264-7, 2016 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26915939
14.
MYOC mutations in black south african patients with primary open-angle glaucoma: genetic testing and cascade screening.
Ophthalmic Genet
; 36(1): 31-8, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25330346
15.
Testing for haemoglobinopathies in Johannesburg, South Africa: a 30-year review.
S Afr Med J
; 103(12 Suppl 1): 989-93, 2013 Oct 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-24300645
16.
Fanconi anaemia in black South African patients heterozygous for the FANCG c.637-643delTACCGCC founder mutation.
S Afr Med J
; 103(12 Suppl 1): 970-3, 2013 Oct 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-24300640