Bohring-Opitz syndrome: MedlinePlus Genetics
Ultra-Rare Syndrome Celebrates Its Day in the Spotlight — Bohring-Opitz Syndrome Foundation, Inc.
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
Lennon — Bohring-Opitz Syndrome Foundation, Inc.
Talynn's Diagnoses: Bohring- Opitz Syndrome - Global Genes
Bohring–Opitz (Oberklaid–Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis | European Journal of Human Genetics
Frontiers | A de novo Variant of ASXL1 Is Associated With an Atypical Phenotype of Bohring-Opitz Syndrome: Case Report and Literature Review | Pediatrics
Tiny and Fierce: Living with Bohring-Opitz Syndrome | A Journey from Undiagnosed to Ultra-Rare
Infantile high myopia in Bohring-Opitz syndrome - Journal of American Association for Pediatric Ophthalmology and Strabismus {JAAPOS}
Bohring-Opitz syndrome: MedlinePlus Genetics
Bohring-Opitz Syndrome OMIM# 605039 - FDNA
Bohring-Opitz Syndrome Foundation, Inc. Bohring-Opitz Syndrome Foundation, Inc.
Layla's Story - Bohring Opitz Syndrome - BOS - Home | Facebook
Darling Anne
Features – Bohring-Opitz Syndrome
The Bohring-Opitz Syndrome Ribbon. Gold & Denim www.facebook.com/BohringOpitz | Medical history, Awareness, Syndrome
Alexa Dodge is fundraising for 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](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
Bohring–Opitz (Oberklaid–Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis | European Journal of Human Genetics
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati Children's Blog
BOHRING-OPITZ SYNDROME Bohring–Opitz syndrome (BOS) is a medical syndrome characterised by characteristi… | Failure to thrive, Magnetic resonance imaging, 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
What is Bohring-Opitz Syndrome?
Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance. - Abstract - Europe PMC
Rare Leader: Taylor Gurganus, Chair and Co-Founder, Bohring-Opitz Syndrome Foundation - Global Genes
