Rosemary — Bohring-Opitz Syndrome Foundation, Inc.
Darling Anne
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew
Bohring-Opitz Syndrome | Bonfire
Bohring-Opitz Syndrome | For Little Eyes
Bohring–Opitz (Oberklaid–Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis | European Journal of Human Genetics
Lennon — Bohring-Opitz Syndrome Foundation, Inc.
What is Bohring-Opitz Syndrome?
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome | Nature Genetics
Comparison of photographs of patients with Bohring-Opitz syndrome (BOS)... | Download Scientific Diagram
Sienna — 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
Bohring–Opitz (Oberklaid–Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis | European Journal of Human Genetics
Main features of Bohring-Opitz Syndrome – Bohring-Opitz Syndrome
Bohring–Opitz (Oberklaid–Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis | European Journal of Human Genetics
Bohring-Opitz syndrome: MedlinePlus Genetics
Bohring Opitz Syndrome - YouTube
Tiny and Fierce: Living with Bohring-Opitz Syndrome | A Journey from Undiagnosed to Ultra-Rare
Bohring-Opitz Syndrome Awareness Day | For Little Eyes
About Bohring-Opitz Syndrome (ASXL1) — ASXL Rare Research Endowment Foundation
Hurricane Hudson's Journey - 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
Bohring-Opitz Syndrome Foundation, Inc. - Bohring-Opitz Syndrome is a rare genetic syndrome that is caused by a mutation in the ASXL1 gene. Here are some photos of children with BOS when they
