Delineating the phenotypic spectrum of Bainbridge-Ropers syndrome: 12 new patients with de novo, heterozygous, loss-of-function mutations in ASXL3 and review of published literature | Journal of Medical Genetics
Della — Leo's Lighthouse
Family finds answers, hope after discovery of rare genetic disorder
Della — Leo's Lighthouse
Novel Nonsense Mutation in ASXL3 causing Bainbridge-Ropers Syndrome
Bainbridge-Ropers Syndrome and ASXL3 Families | Facebook
Bainbridge-Ropers Syndrome Pontiac, MI - EURO-THERAPIES
SPARK for Autism | On the Edge of Autism
A Unique Physical Therapy Approach for my Son with Bainbridge-Ropers Syndrome - EURO-THERAPIES
About Bainbridge-Ropers Syndrome (ASXL3) — ASXL Rare Research Endowment Foundation
Clinical presentation of four subjects. (A, B) Subject 2 aged (A) 1... | Download Scientific Diagram
About Bainbridge-Ropers Syndrome (ASXL3) — ASXL Rare Research Endowment Foundation
Bainbridge–Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition | European Journal of Human Genetics
Bainbridge-Ropers syndrome (BRPS)
Familial Bainbridge‐Ropers syndrome: Report of familial ASXL3 inheritance and a milder phenotype - Schirwani - 2023 - American Journal of Medical Genetics Part A - Wiley Online Library
A Texas teen couldn't speak with his sister, so he created an app to give her a voice | CNN
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Further expanding the clinical phenotype in Bainbridge-Ropers syndrome and dissecting genotype-phenotype correlation in the ASXL3 mutational cluster regions - ScienceDirect
De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype
About Bainbridge-Ropers Syndrome (ASXL3) — ASXL Rare Research Endowment Foundation
Upworthy on Twitter: "The Calder family has two kids - a nonverbal 14-year-old named Della with a rare genetic condition called Bainbridge-Ropers Syndrome, and her 16-year-old brother Archer, who coded an app
Family finds answers, hope after discovery of rare genetic disorder
Bainbridge-Ropers Syndrome OMIM# 615485 - FDNA
About BRS — Leo's Lighthouse
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Bainbridge-ropers syndrome caused by loss-of-function variants in ASXL3: Clinical abnormalities, medical imaging features, and gene variation in infancy of case report | BMC Pediatrics | Full Text
Bainbridge-Ropers syndrome (BRPS)
