Joyce E. Fox
Pediatrics
Lijmc-dept Of Pediatrics Human Genetics
269-01 76th Avenue
New Hyde Park, NY 11040
269-01 76th Avenue
New Hyde Park, NY 11040
Last Updated: 09/26/2026
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Found 6 publications
Highly Sensitive Blocker Displacement Amplification and Droplet Digital PCR Reveal Low-Level Parental FOXF1 Somatic Mosaicism in Families with Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins.
Journal: The Journal of molecular diagnostics : JMD
Published: August 09, 2019
Prevention of Leber congenital amaurosis through preimplantation genetic diagnosis.
Journal: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus
Published: February 20, 2017
Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins.
Journal: Human genetics
Published: January 08, 2016
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.
Journal: American journal of human genetics
Published: June 04, 2015
First human treatment with investigational rhGUS enzyme replacement therapy in an advanced stage MPS VII patient.
Journal: Molecular genetics and metabolism
Published: September 11, 2014
Severe obesity and diabetes insipidus in a patient with PCSK1 deficiency.
Journal: Molecular genetics and metabolism
Published: February 08, 2013
Showing 1-6 of 6
Last Updated: 09/26/2026