Last Updated: 09/26/2026
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Found 10 publications
Racial Differences in Utilization of and Factors Contributing to the Use of Knee Replacement Surgery as a Treatment for Severe Knee Osteoarthritis: A Scoping Review.
Journal: Osteoarthritis and cartilage open
Published: November 21, 2025
Association of clinical outcomes in metastatic breast cancer patients with circulating tumour cell and circulating cell-free DNA.
Journal: European journal of cancer (Oxford, England : 1990)
Published: June 05, 2018
Correction to: A zebrafish model of foxe3 deficiency demonstrates lens and eye defects with dysregulation of key genes involved in cataract formation in humans.
Journal: Human genetics
Published: May 13, 2018
Biallelic sequence variants in INTS1 in patients with developmental delays, cataracts, and craniofacial anomalies.
Journal: European journal of human genetics : EJHG
Published: March 22, 2018
A zebrafish model of foxe3 deficiency demonstrates lens and eye defects with dysregulation of key genes involved in cataract formation in humans.
Journal: Human genetics
Published: January 11, 2018
Variants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome.
Journal: European journal of human genetics : EJHG
Published: April 11, 2017
A recurrent, non-penetrant sequence variant, p.Arg266Cys in Growth/Differentiation Factor 3 (GDF3) in a female with unilateral anophthalmia and skeletal anomalies.
Journal: American journal of ophthalmology case reports
Published: April 29, 2016
Expansion of phenotype and genotypic data in CRB2-related syndrome.
Journal: European journal of human genetics : EJHG
Published: November 20, 2015
Showing 1-10 of 10
Last Updated: 09/26/2026