Frontiers | A de novo Variant of ASXL1 Is Associated With an Atypical Phenotype of Bohring-Opitz Syndrome: Case Report and Literature Review
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
Talynn's Diagnoses: Bohring- Opitz Syndrome - Global Genes
Bohring-Opitz syndrome: MedlinePlus Genetics
About Bohring-Opitz Syndrome (ASXL1) — ASXL Rare Research Endowment Foundation
What's day-to-day life like with Bohring-Opitz Syndrome? | Tiny and Fierce: Living with Bohring-Opitz Syndrome
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 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 Journey: Bohring-Opitz Syndrome Awareness Day - Sarah Halstead
What is Bohring-Opitz Syndrome?
Lennon — Bohring-Opitz Syndrome Foundation, Inc.
Bohring–Opitz (Oberklaid–Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis | European Journal of Human 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
ISMKI Wilayah 4 on Twitter: "[WORLD BOHRING-OPITZ SYNDROME] Bohring-Opitz Syndrome Awareness Day takes place on April 6th each year. Bohring–Opitz syndrome (BOS) is a medical syndrome caused by a mutation in the
Bohring–Opitz (Oberklaid–Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis | European Journal of Human Genetics
Bohring Opitz Syndrome - YouTube
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome | Nature Genetics
Annessia's Army Against Bohring-Opitz Syndrome & Epilepsy
Tiny and Fierce: Living with Bohring-Opitz Syndrome | A Journey from Undiagnosed to Ultra-Rare