Tiny and Fierce: Living with Bohring-Opitz Syndrome | A Journey from Undiagnosed to Ultra-Rare
BOS - Bohring-Opitz-Syndrom - Jannis Loewenherz
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati Children's Blog
De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome. - Abstract - Europe PMC
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome | Genome Medicine | Full Text
Other Cases which are related with BOS – Bohring-Opitz Syndrome
Trigonocephalie
Bohring-Opitz syndrome (Concept Id: C0796232)
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome | Nature Genetics
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
جوريس أندريه ڤلتمان - Wikiwand
Global Journal of Medical Research
Bohring-Opitz syndrome: MedlinePlus Genetics
Tiny and Fierce: Living with Bohring-Opitz Syndrome | A Journey from Undiagnosed to Ultra-Rare
Bohring-Opitz sendromu - Vikipedi
BOS - Bohring-Opitz-Syndrom - Jannis Loewenherz
Hexadaktylie
Bohring-Opitz (Oberklaid-Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis. - Abstract - Europe PMC
Main features of Bohring-Opitz Syndrome – Bohring-Opitz Syndrome
John M. Opitz - Wikipedia
Bohring-Opitz sendromu
Bohring Opitz Syndrome - YouTube
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
Bohring-Opitz Syndrome
Trigonocephalie - Wikiwand
Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies | PLOS Genetics
