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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

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}

Comparison of photographs of patients with Bohring-Opitz syndrome (BOS)...  | Download Scientific Diagram
Comparison of photographs of patients with Bohring-Opitz syndrome (BOS)... | Download Scientific Diagram

Bohring-Opitz Syndrome
Bohring-Opitz Syndrome

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

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

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

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 Syndrome OMIM# 605039 - FDNA
Bohring-Opitz Syndrome OMIM# 605039 - FDNA

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

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

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

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

Comparison of photographs of patients with Bohring-Opitz syndrome (BOS)...  | Download Scientific Diagram
Comparison of photographs of patients with Bohring-Opitz syndrome (BOS)... | Download Scientific Diagram

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

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.

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

Bohring-Opitz Syndrome Awareness Day | For Little Eyes
Bohring-Opitz Syndrome Awareness Day | For Little Eyes

Bohring-Opitz Awareness Day - Firefly Blog
Bohring-Opitz Awareness Day - Firefly Blog

Rare Leader: Taylor Gurganus, Chair and Co-Founder, Bohring-Opitz Syndrome  Foundation - Global Genes
Rare Leader: Taylor Gurganus, Chair and Co-Founder, Bohring-Opitz Syndrome Foundation - Global Genes

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

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

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

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

Bohring- Opitz Syndrome Archives - Global Genes
Bohring- Opitz Syndrome Archives - Global Genes