Bohring–Opitz (Oberklaid–Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis | European Journal of Human Genetics
Comparison of photographs of patients with Bohring-Opitz syndrome (BOS)... | Download Scientific Diagram
Hurricane Hudson's Journey - Bohring Opitz Syndrome
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
Novel truncating mutations in ASXL1 identified in two boys with Bohring-Opitz syndrome - ScienceDirect
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
![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](https://pbs.twimg.com/media/EU5YDkxVAAEHWcA.jpg "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")
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
Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance. - Abstract - Europe PMC
New cases of Bohring–Opitz syndrome, update, and critical review of the literature - Bohring - 2006 - 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
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
Talynn's Diagnoses: Bohring- Opitz Syndrome - Global Genes
Features – Bohring-Opitz Syndrome
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew
Darling Anne
About Bohring-Opitz Syndrome (ASXL1) — ASXL Rare Research Endowment Foundation
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
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome | Nature Genetics
Bohring-Opitz Syndrome
Rosemary — 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 | For Little Eyes
Sienna — Bohring-Opitz Syndrome Foundation, Inc.
