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
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
From Undiagnosed to Bohring-Opitz Syndrome: Finding Our Crew - Cincinnati Children's Blog
Features – 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
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome | Nature Genetics
Comparison of photographs of patients with Bohring-Opitz syndrome (BOS)... | Download Scientific Diagram
Bohring-Opitz Syndrome
About Bohring-Opitz Syndrome | Tiny and Fierce: Living with Bohring-Opitz Syndrome
American Journal of Medical Genetics Part A: Vol 176, No 5
Unusual Brain and/or Neuromuscular Findings with Associated Defects | Obgyn Key
BOS - Bohring-Opitz-Syndrom - Jannis Loewenherz
Bohring-Opitz Syndrome Receives International Attention — Bohring-Opitz Syndrome Foundation, Inc.
Medical Publications – Bohring-Opitz Syndrome
Talynn's Diagnoses: Bohring- Opitz Syndrome - Global Genes
Comparison of photographs of patients with Bohring-Opitz syndrome (BOS)... | Download Scientific Diagram
Bohring-Opitz Syndrome OMIM# 605039 - FDNA
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
Infantile high myopia in Bohring-Opitz syndrome - Journal of American Association for Pediatric Ophthalmology and Strabismus {JAAPOS}
Neue syndromale Krankheitsbilder mit Mikrozephalie | 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
Oktober We Wear Blau & Gelb Down Syndrom Kürbis | Etsy Schweiz
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome - Document - Gale Academic OneFile
Bohring-Opitz syndrome: MedlinePlus Genetics
