Publications by authors named "Allison D Britt"

Claim this Profile
E
Expansion of the Phenotype of Lymphatic Anomalies Caused by Somatic Activating BRAF Variant.
Michael D Fox, Sumukh Kumar, Allison D Britt, Abhay S Srinivasan, Lea F Surrey

Pediatr Blood Cancer· November 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical Phenotypes of a Pediatric Cohort with -Related Hereditary Hemorrhagic Telangiectasia.
Owen Oliver, Allison D Britt, Alexandra J Borst, Elizabeth Goldmuntz, Nihal Bakeer

J Clin Med· May 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Expanding Genetic Counselor Roles: A Model for Global Research Development.
Colleen C Muraresku, Elizabeth M McCormick, Lydia Rockart, T Blaine Crowley, Stephanie Asher, Allison D Britt

Genes (Basel)· July 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genomic profiling informs diagnoses and treatment in vascular anomalies.
Dong Li, Sarah E Sheppard, Michael E March, Mark R Battig, Lea F Surrey, Allison D Britt

Nat Med· June 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mosaic pathogenic variants in AKT3 cause capillary malformation and undergrowth.
Amber Bolli, Bede Nriagu, Allison D Britt, Anjali D Toole, James Treat

Am J Med Genet A· May 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genotypic and phenotypic variability of 22q11.2 microdeletions - an institutional experience.
Gabrielle C Manno, Gabrielle S Segal, Alexander Yu, Fangling Xu, Joseph W Ray, Allison D Britt

AIMS Mol Sci· December 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genotypic and phenotypic variability of 22q11.2 microduplications: An institutional experience.
Alexander Yu, Donald Turbiville, Fangling Xu, Joseph W Ray, Allison D Britt

Am J Med Genet A· November 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A De novo HDAC2 variant in a patient with features consistent with Cornelia de Lange syndrome phenotype.
Victoria F Wagner, Paul R Hillman, Allison D Britt, Joseph W Ray, Laura S Farach

Am J Med Genet A· May 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis