Detalhe da pesquisa
1.
ALG13 X-linked intellectual disability: New variants, glycosylation analysis, and expanded phenotypes.
J Inherit Metab Dis
; 44(4): 1001-1012, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33734437
2.
Experiences with offering pro bono medical genetics services in the West Indies: Benefits to patients, physicians, and the community.
Am J Med Genet C Semin Med Genet
; 184(4): 1030-1041, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33274544
3.
Clinical, Serological, and Molecular Observations from a Case Series Study during the Asian Lineage Zika Virus Outbreak in Grenada during 2016.
Can J Infect Dis Med Microbiol
; 2018: 4635647, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29623138
4.
Erratum: Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology.
HGG Adv
; 4(1): 100168, 2023 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36583168
5.
A novel unbalanced translocation between chromosomes 5p and 18q leading to dysmorphology and global developmental delay.
Mol Genet Genomic Med
; 10(4): e1900, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35189041
6.
Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology.
HGG Adv
; 3(3): 100102, 2022 Jul 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-35469323
7.
Presentation and care of a family with Huntington disease in a resource-limited community.
J Clin Mov Disord
; 4: 4, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28413688
8.
Clinical and Serological Insights from the Asian Lineage Chikungunya Outbreak in Grenada, 2014: An Observational Study.
Am J Trop Med Hyg
; 95(4): 890-893, 2016 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27527629