PDF) Umblical hernia, hypertelorism, sensorineural deafness: Is it Donnai� Barrow syndrome? | Ersel Onrat - Academia.edu
Patient 1. a: Note hypertelorism, marked underorbital creases, short... | Download Scientific Diagram
A 56-year-old female patient with facio-oculo-acoustico-renal syndrome (FOAR) syndrome. Report on the natural history and of a novel mutation. | Semantic Scholar
Ocular Manifestations of Donnai Barrow Syndrome | European Journal of Medical and Health Sciences
Donnai-Barrow Syndrome Support
Tributes paid to 29-year-old who made people 'smile and laugh' - LancsLive
Patient Stories: Cordelia C — Dankmeyer, Inc.
Meet the Garcias | Jerry Garcia Ministries
Donnai– Barrow Syndrome in Two Sisters with a Homozygous LRP2 Mutation and Renal Dysfunction. Integral Management of the Disease with Review of the Literature.
Phenotype resembling Donnai–Barrow syndrome in a patient with 9qter;16qter unbalanced translocation - Ferrero - 2006 - American Journal of Medical Genetics Part A - Wiley Online Library
Donnai-Barrow syndrome: MedlinePlus Genetics
Persistent pupillary membrane, strabismus, and optic nerve hypoplasia in Donnai-Barrow syndrome - ScienceDirect
Michelle Rheault on Twitter: "Donnai-Barrow Syndrome: absence of megalin. #aspn19 https://t.co/bQBlMKQFob https://t.co/LhxNfaTfYV" / Twitter
Donnai-Barrow Syndrome | Hereditary Ocular Diseases
Tributes paid to 29-year-old who made people 'smile and laugh' - LancsLive
Donnai–Barrow syndrome (DBS/FOAR) in a child with a homozygous LRP2 mutation due to complete chromosome 2 paternal isodisomy - Kantarci - 2008 - American Journal of Medical Genetics Part A - Wiley Online Library
JPM | Free Full-Text | Stickler Syndrome: A Review of Clinical Manifestations and the Genetics Evaluation
Donnai-Barrow Syndrome Support
Ocular Manifestations of Donnai Barrow Syndrome
