About Bohring-Opitz Syndrome (ASXL1) — ASXL Rare Research Endowment Foundation
Bohring-Opitz Syndrome | For Little Eyes
Bohring-Opitz syndrome: MedlinePlus Genetics
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
Tiny and Fierce: Living with Bohring-Opitz Syndrome | A Journey from Undiagnosed to Ultra-Rare
What's day-to-day life like with Bohring-Opitz Syndrome? | Tiny and Fierce: Living with Bohring-Opitz Syndrome
About Bohring-Opitz Syndrome (ASXL1) — ASXL Rare Research Endowment Foundation
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
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew
Annessia's Army Against Bohring-Opitz Syndrome & Epilepsy
Eva — Bohring-Opitz Syndrome Foundation, Inc.
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 - YouTube
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
Talynn's Diagnoses: Bohring- Opitz Syndrome - Global Genes
Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring–Opitz syndromes - Urreizti - 2016 - American Journal of Medical Genetics Part A - Wiley Online Library
Bohring-Opitz Syndrome
Sienna — Bohring-Opitz Syndrome Foundation, Inc.
Novel truncating mutations in ASXL1 identified in two boys with Bohring-Opitz syndrome - ScienceDirect
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
Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance. - Abstract - Europe PMC
Features – Bohring-Opitz Syndrome
Darling Anne
Talynn's Journey: Bohring-Opitz Syndrome Awareness Day - Sarah Halstead
