About Bohring-Opitz Syndrome | Tiny and Fierce: Living with Bohring-Opitz Syndrome
Oktober We Wear Blau & Gelb Down Syndrom Kürbis | Etsy Schweiz
BOS - Bohring-Opitz-Syndrom - Jannis Loewenherz
Bainbridge-ropers syndrome caused by loss-of-function variants in ASXL3: Clinical abnormalities, medical imaging features, and gene variation in infancy of case report | SpringerLink
Bohring-Opitz Syndrome now has an AWESOME Infographic! This was created by a BOS mom and she even made it in multiple lan… | Infant mortality, Infographic, Syndrome
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati Children's Blog
Infantile high myopia in Bohring-Opitz syndrome - Journal of American Association for Pediatric Ophthalmology and Strabismus {JAAPOS}
Bi-allelic c.181_183delTGT in BTB domain of KLHL7 is associated with overlapping phenotypes of Crisponi/CISS1-like and Bohring-Opitz like syndrome - ScienceDirect
Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring–Opitz syndromes - Urreizti - 2016 - American Journal of Medical Genetics Part A - Wiley Online Library
Bohring Opitz syndrome causes, symptoms, diagnosis, treatment & prognosis
Bohring-Opitz Syndrome OMIM# 605039 - FDNA
Features – Bohring-Opitz Syndrome
Comparison of photographs of patients with Bohring-Opitz syndrome (BOS)... | Download Scientific Diagram
Cause – Bohring-Opitz Syndrome
Bohring-Opitz syndrome: MedlinePlus Genetics
Bohring-Opitz Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome - Document - Gale Academic OneFile
American Journal of Medical Genetics Part A: Vol 176, No 5
Talynn's Diagnoses: Bohring- Opitz Syndrome - Global Genes
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Seltene Tumordispositionssyndrome mit Manifestation im Kindesalter | SpringerLink
Unusual Brain and/or Neuromuscular Findings with Associated Defects | Obgyn Key
Neue syndromale Krankheitsbilder mit Mikrozephalie | SpringerLink
