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1.
Common and Founder Mutations for Monogenic Traits in Sub-Saharan African Populations.
Annu Rev Genomics Hum Genet
; 19: 149-175, 2018 08 31.
Article
in English
| MEDLINE | ID: mdl-30169122
2.
Location of the appendix in the gravid patient.
J Emerg Med
; 46(5): 741-4, 2014 May.
Article
in English
| MEDLINE | ID: mdl-24484624
3.
A feasible molecular diagnostic strategy for rare genetic disorders within resource-constrained environments.
J Community Genet
; 15(1): 39-48, 2024 Feb.
Article
in English
| MEDLINE | ID: mdl-37815686
4.
Mutation profiling in South African patients with Cornelia de Lange syndrome phenotype.
Mol Genet Genomic Med
; 12(1): e2342, 2024 Jan.
Article
in English
| MEDLINE | ID: mdl-38284454
5.
Identifying the genetic causes of developmental disorders and intellectual disability in Africa: a systematic literature review.
Front Genet
; 14: 1137922, 2023.
Article
in English
| MEDLINE | ID: mdl-37234869
6.
Coronavirus Host Genomics Study: South Africa (COVIGen-SA).
Glob Health Epidemiol Genom
; 2022: 7405349, 2022.
Article
in English
| MEDLINE | ID: mdl-36263375
7.
Breast cancer in high-risk Afrikaner families: Is BRCA founder mutation testing sufficient?
S Afr Med J
; 106(3): 264-7, 2016 Feb 03.
Article
in English
| MEDLINE | ID: mdl-26915939
8.
Loss of seven-up from Drosophila R1/R6 photoreceptors reveals a stochastic fate choice that is normally biased by Notch.
Development
; 135(4): 707-15, 2008 Feb.
Article
in English
| MEDLINE | ID: mdl-18199577
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