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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
![Clinical presentation of four subjects. (A, B) Subject 2 aged (A) 1... | Download Scientific Diagram Clinical presentation of four subjects. (A, B) Subject 2 aged (A) 1... | Download Scientific Diagram](https://www.researchgate.net/publication/235403612/figure/fig1/AS:214016518561792@1428036922413/Clinical-presentation-of-four-subjects-A-B-Subject-2-aged-A-1-month-and-B-385.png)
Clinical presentation of four subjects. (A, B) Subject 2 aged (A) 1... | Download Scientific Diagram
![Bainbridge–Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition | European Journal of Human Genetics Bainbridge–Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition | European Journal of Human Genetics](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fejhg.2016.165/MediaObjects/41431_2017_Article_BFejhg2016165_Fig1_HTML.jpg)
Bainbridge–Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition | European Journal of Human Genetics
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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
![Further expanding the clinical phenotype in Bainbridge-Ropers syndrome and dissecting genotype-phenotype correlation in the ASXL3 mutational cluster regions - ScienceDirect Further expanding the clinical phenotype in Bainbridge-Ropers syndrome and dissecting genotype-phenotype correlation in the ASXL3 mutational cluster regions - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S176972122030817X-gr1.jpg)
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
![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 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](https://pbs.twimg.com/media/FCFLE2xVgAAFGfe.jpg:large)
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
![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 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](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs12887-020-02027-7/MediaObjects/12887_2020_2027_Fig1_HTML.png)
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
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