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Talynn — Bohring-Opitz Syndrome Foundation, Inc.
Talynn — Bohring-Opitz Syndrome Foundation, Inc.

The Bohring-Opitz Syndrome Ribbon. Gold & Denim  www.facebook.com/BohringOpitz | Medical history, Awareness, Syndrome
The Bohring-Opitz Syndrome Ribbon. Gold & Denim www.facebook.com/BohringOpitz | Medical history, Awareness, Syndrome

What's day-to-day life like with Bohring-Opitz Syndrome? | Tiny and Fierce:  Living with Bohring-Opitz Syndrome
What's day-to-day life like with Bohring-Opitz Syndrome? | Tiny and Fierce: Living with Bohring-Opitz Syndrome

Frontiers | A de novo Variant of ASXL1 Is Associated With an Atypical  Phenotype of Bohring-Opitz Syndrome: Case Report and Literature Review |  Pediatrics
Frontiers | A de novo Variant of ASXL1 Is Associated With an Atypical Phenotype of Bohring-Opitz Syndrome: Case Report and Literature Review | Pediatrics

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

Darling Anne
Darling Anne

Clinical management of patients with ASXL1 mutations and Bohring-Opitz  syndrome, emphasizing the need for Wilms tumor surveillance. - Abstract -  Europe PMC
Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance. - Abstract - Europe PMC

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
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

Bohring-Opitz syndrome: MedlinePlus Genetics
Bohring-Opitz syndrome: MedlinePlus Genetics

For the Love of Lauren Marie Graham ~ Bohring Opitz Syndrome - Alaska -  Posts | Facebook
For the Love of Lauren Marie Graham ~ Bohring Opitz Syndrome - Alaska - Posts | Facebook

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
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

From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati  Children's Blog
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati Children's Blog

Tiny and Fierce: Living with Bohring-Opitz Syndrome | A Journey from  Undiagnosed to Ultra-Rare
Tiny and Fierce: Living with Bohring-Opitz Syndrome | A Journey from Undiagnosed to Ultra-Rare

BOHRING-OPITZ SYNDROME Bohring–Opitz syndrome (BOS) is a medical syndrome  characterised by characteristi… | Failure to thrive, Magnetic resonance  imaging, Syndrome
BOHRING-OPITZ SYNDROME Bohring–Opitz syndrome (BOS) is a medical syndrome characterised by characteristi… | Failure to thrive, Magnetic resonance imaging, Syndrome

Features – Bohring-Opitz Syndrome
Features – Bohring-Opitz Syndrome

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

Infantile high myopia in Bohring-Opitz syndrome - Journal of American  Association for Pediatric Ophthalmology and Strabismus {JAAPOS}
Infantile high myopia in Bohring-Opitz syndrome - Journal of American Association for Pediatric Ophthalmology and Strabismus {JAAPOS}

From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati  Children's Blog
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati Children's Blog

Ultra-Rare Syndrome Celebrates Its Day in the Spotlight — Bohring-Opitz  Syndrome Foundation, Inc.
Ultra-Rare Syndrome Celebrates Its Day in the Spotlight — Bohring-Opitz Syndrome Foundation, Inc.

Lennon — Bohring-Opitz Syndrome Foundation, Inc.
Lennon — Bohring-Opitz Syndrome Foundation, Inc.

Clinical management of patients with ASXL1 mutations and Bohring-Opitz  syndrome, emphasizing the need for Wilms tumor surveillance. - Abstract -  Europe PMC
Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance. - Abstract - Europe PMC

Main features of Bohring-Opitz Syndrome – Bohring-Opitz Syndrome
Main features of Bohring-Opitz Syndrome – Bohring-Opitz Syndrome

Bohring-Opitz syndrome: MedlinePlus Genetics
Bohring-Opitz syndrome: MedlinePlus Genetics

Alexa Dodge is fundraising for Bohring-Opitz Syndrome Foundation Inc
Alexa Dodge is fundraising for Bohring-Opitz Syndrome Foundation Inc

De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome | Nature  Genetics
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome | Nature Genetics