Bohring–Opitz (Oberklaid–Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis | European Journal of Human Genetics
Features – Bohring-Opitz Syndrome
Bohring- Opitz Syndrome Archives - Global Genes
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati Children's Blog
For the Love of Lauren Marie Graham ~ Bohring Opitz Syndrome - Alaska - Posts | Facebook
Darling Anne
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
Bohring-Opitz Syndrome Awareness Day | For Little Eyes
What is Bohring-Opitz Syndrome?
BOHRING-OPITZ SYNDROME Bohring–Opitz syndrome (BOS) is a medical syndrome characterised by characteristi… | Failure to thrive, Magnetic resonance imaging, Syndrome
Bohring-Opitz Awareness Day - Firefly Blog
Ultra-Rare Syndrome Celebrates Its Day in the Spotlight — Bohring-Opitz Syndrome Foundation, Inc.
Bohring-Opitz syndrome: MedlinePlus Genetics
Main features of Bohring-Opitz Syndrome – Bohring-Opitz Syndrome
Infantile high myopia in Bohring-Opitz syndrome - Journal of American Association for Pediatric Ophthalmology and Strabismus {JAAPOS}
Rare Leader: Taylor Gurganus, Chair and Co-Founder, Bohring-Opitz Syndrome Foundation - Global Genes
Bohring-Opitz Syndrome Foundation, Inc. Bohring-Opitz Syndrome Foundation, Inc.
Bohring-Opitz syndrome: MedlinePlus Genetics
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
Comparison of photographs of patients with Bohring-Opitz syndrome (BOS)... | Download Scientific Diagram
The Bohring-Opitz Syndrome Ribbon. Gold & Denim www.facebook.com/BohringOpitz | Medical history, Awareness, Syndrome
Comparison of photographs of patients with Bohring-Opitz syndrome (BOS)... | Download Scientific Diagram
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome | Nature Genetics
Bohring–Opitz (Oberklaid–Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis | European Journal of Human Genetics
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati Children's Blog
Alexa Dodge is fundraising for 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