De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome | Nature Genetics
About Bohring-Opitz Syndrome | Tiny and Fierce: Living with Bohring-Opitz Syndrome
Features – Bohring-Opitz Syndrome
Comparison of photographs of patients with Bohring-Opitz syndrome (BOS)... | Download Scientific Diagram
Bohring–Opitz (Oberklaid–Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis | European Journal of Human Genetics
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
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 OMIM# 605039 - FDNA
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
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
Bohring–Opitz (Oberklaid–Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis | European Journal of Human Genetics
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Unusual Brain and/or Neuromuscular Findings with Associated Defects | Obgyn Key
Seltene Tumordispositionssyndrome mit Manifestation im Kindesalter | SpringerLink
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
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
Opitz Gbbb Syndrome, Type I disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Oktober We Wear Blau & Gelb Down Syndrom Kürbis | Etsy Schweiz
Medical Publications – Bohring-Opitz Syndrome
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
Neue syndromale Krankheitsbilder mit Mikrozephalie | SpringerLink
