The Bohring-Opitz Syndrome Ribbon. Gold & Denim www.facebook.com/BohringOpitz | Medical history, Awareness, Syndrome
What's day-to-day life like with Bohring-Opitz Syndrome? | Tiny and Fierce: Living with Bohring-Opitz Syndrome
Frontiers | A de novo Variant of ASXL1 Is Associated With an Atypical Phenotype of Bohring-Opitz Syndrome: Case Report and Literature Review | Pediatrics
Bohring–Opitz (Oberklaid–Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis | European Journal of Human Genetics
Darling Anne
Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance. - Abstract - Europe PMC
Talynn's Journey:BOS on Twitter: "Help raise awareness about Bohring-Opitz Syndrome. Talynn is the youngest living in the US! http://t.co/NE0qnRdl5o http://t.co/wCpSKMbq7L" / Twitter
Bohring-Opitz syndrome: MedlinePlus Genetics
For the Love of Lauren Marie Graham ~ Bohring Opitz Syndrome - Alaska - Posts | Facebook
Extending the phenotypic spectrum of Bohring‐Opitz syndrome: Mild case confirmed by functional studies - Leon - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati Children's Blog
Tiny and Fierce: Living with Bohring-Opitz Syndrome | A Journey from Undiagnosed to Ultra-Rare
BOHRING-OPITZ SYNDROME Bohring–Opitz syndrome (BOS) is a medical syndrome characterised by characteristi… | Failure to thrive, Magnetic resonance imaging, Syndrome
Features – Bohring-Opitz Syndrome
Bohring–Opitz (Oberklaid–Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis | European Journal of Human Genetics
Infantile high myopia in Bohring-Opitz syndrome - Journal of American Association for Pediatric Ophthalmology and Strabismus {JAAPOS}
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati Children's Blog
Ultra-Rare Syndrome Celebrates Its Day in the Spotlight — Bohring-Opitz Syndrome Foundation, Inc.
Lennon — Bohring-Opitz Syndrome Foundation, Inc.
Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance. - Abstract - Europe PMC
Main features of Bohring-Opitz Syndrome – Bohring-Opitz Syndrome
Bohring-Opitz syndrome: MedlinePlus Genetics
Alexa Dodge is fundraising for Bohring-Opitz Syndrome Foundation Inc
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome | Nature Genetics