Katherine R. Yearwood - Publications

Erratum: Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology.

Journal: HGG advances

Published: December 30, 2022

Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology.

Journal: HGG advances

Published: December 14, 2021

A novel unbalanced translocation between chromosomes 5p and 18q leading to dysmorphology and global developmental delay.

Journal: Molecular genetics & genomic medicine

Published: July 27, 2021

ALG13 X-linked intellectual disability: New variants, glycosylation analysis, and expanded phenotypes.

Journal: Journal of inherited metabolic disease

Published: October 22, 2020

Experiences with offering pro bono medical genetics services in the West Indies: Benefits to patients, physicians, and the community.

Journal: American journal of medical genetics. Part C, Seminars in medical genetics

Published: October 13, 2020

Clinical, Serological, and Molecular Observations from a Case Series Study during the Asian Lineage Zika Virus Outbreak in Grenada during 2016.

Journal: The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale

Published: July 24, 2017

Presentation and care of a family with Huntington disease in a resource-limited community.

Journal: Journal of clinical movement disorders

Published: September 13, 2016

Clinical and Serological Insights from the Asian Lineage Chikungunya Outbreak in Grenada, 2014: An Observational Study.

Journal: The American journal of tropical medicine and hygiene

Published: February 16, 2016