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
Lennon — Bohring-Opitz Syndrome Foundation, Inc.
Talynn's Journey: Bohring-Opitz Syndrome Awareness Day - Sarah Halstead
Meet Evelyn
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati Children's Blog
Rare Leader: Taylor Gurganus, Chair and Co-Founder, Bohring-Opitz Syndrome Foundation - Global Genes
Bohring-Opitz Syndrome Foundation, Inc. Bohring-Opitz Syndrome Foundation, Inc.
Bohring-Opitz syndrome: MedlinePlus Genetics
Layla's Story - Bohring Opitz Syndrome - BOS | Facebook
Frontiers | A de novo Variant of ASXL1 Is Associated With an Atypical Phenotype of Bohring-Opitz Syndrome: Case Report and Literature Review
Ultra-Rare Syndrome Celebrates Its Day in the Spotlight — Bohring-Opitz Syndrome Foundation, Inc.
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati Children's Blog
Comparison of photographs of patients with Bohring-Opitz syndrome (BOS)... | Download Scientific Diagram
Bohring–Opitz (Oberklaid–Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis | European Journal of Human Genetics
Bohring-Opitz Syndrome
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
BOHRING-OPITZ SYNDROME Bohring–Opitz syndrome (BOS) is a medical syndrome characterised by characteristic craniofacial appearance, fixed contractures of the… | Tıp
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
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome | Nature Genetics
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
Kate Konik is fundraising for Bohring-Opitz Syndrome Foundation Inc
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati Children's Blog
Features – Bohring-Opitz Syndrome
