From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati Children's Blog
John M. Opitz - Wikipedia
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome | Nature Genetics
Trigonocephalie
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome | Genome Medicine | Full Text
Global Journal of Medical Research
Main features of Bohring-Opitz Syndrome – Bohring-Opitz Syndrome
Bohring-Opitz Syndrome
Tiny and Fierce: Living with Bohring-Opitz Syndrome | A Journey from Undiagnosed to Ultra-Rare
Bohring-Opitz Syndrome: Symptoms - YouTube
Bohring Opitz | Flickr
Bohring-Opitz syndrome: MedlinePlus Genetics
Bohring Opitz syndrome causes, symptoms, diagnosis, treatment & prognosis
Trigonocephalie
BOS - Bohring-Opitz-Syndrom - Jannis Loewenherz
Bainbridge-Ropers-Syndrom
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 sendromu
Bainbridge-ropers syndrome caused by loss-of-function variants in ASXL3: Clinical abnormalities, medical imaging features, and gene variation in infancy of case report | BMC Pediatrics | Full Text
Other Cases which are related with BOS – Bohring-Opitz Syndrome
Bohring-Opitz sendromu - Vikipedi
Features – Bohring-Opitz Syndrome
Life with Bohring-Opitz Syndrome | Syndrome, Genetics, Three year olds
Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies | PLOS Genetics
About Bohring-Opitz Syndrome | Tiny and Fierce: Living with Bohring-Opitz Syndrome
