Ultra-Rare Syndrome Celebrates Its Day in the Spotlight — Bohring-Opitz Syndrome Foundation, Inc.
About Bohring-Opitz Syndrome (ASXL1) — ASXL Rare Research Endowment Foundation
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: MedlinePlus Genetics
Main features of Bohring-Opitz Syndrome – Bohring-Opitz Syndrome
Tiny and Fierce: Living with Bohring-Opitz Syndrome | A Journey from Undiagnosed to Ultra-Rare
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:large "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
Bohring–Opitz (Oberklaid–Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis | European Journal of Human Genetics
Kate Konik is fundraising for Bohring-Opitz Syndrome Foundation Inc
About Bohring-Opitz Syndrome (ASXL1) — ASXL Rare Research Endowment Foundation
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
Tiny and Fierce: Living with Bohring-Opitz Syndrome | A Journey from Undiagnosed to Ultra-Rare
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati Children's Blog
Talynn's Journey: Bohring-Opitz Syndrome Awareness Day - Sarah Halstead
Infantile high myopia in 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
Rare Leader: Taylor Gurganus, Chair and Co-Founder, Bohring-Opitz Syndrome Foundation - Global Genes
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati Children's Blog
What is Bohring-Opitz Syndrome?
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati Children's Blog
Bohring-Opitz syndrome: MedlinePlus Genetics
Bohring-Opitz Syndrome
Bohring-Opitz Syndrome Foundation, Inc. Bohring-Opitz Syndrome Foundation, Inc.
Layla's Story - Bohring Opitz Syndrome - BOS | Facebook
Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance. - Abstract - Europe PMC
Lennon — Bohring-Opitz Syndrome Foundation, Inc.
