Patricia L. Gordon
Medical Genetics | Pediatrics
500 University Dr
Mc A410
Hershey, PA 17033
Mc A410
Hershey, PA 17033
Last Updated: 09/26/2026
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Found 8 publications
Erratum: The adolescent health network: A unique approach to sustained adolescent stakeholder engagement - CORRIGENDUM.
Journal: Journal of clinical and translational science
Published: July 02, 2025
Further delineation of the SCAF4-associated neurodevelopmental disorder.
Journal: European journal of human genetics : EJHG
Published: April 23, 2024
The adolescent health network: A unique approach to sustained adolescent stakeholder engagement.
Journal: Journal of clinical and translational science
Published: August 16, 2023
Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 02, 2021
Newborn Screening for Pompe Disease: Pennsylvania Experience.
Journal: International journal of neonatal screening
Published: October 02, 2020
Strategies to engage lost to follow-up patients with phenylketonuria in the United States: Best practice recommendations.
Journal: Molecular genetics and metabolism reports
Published: January 06, 2020
An interstitial deletion within 9p21.3 and extending beyond CDKN2A predisposes to melanoma, neural system tumours and possible haematological malignancies.
Journal: Journal of medical genetics
Published: August 06, 2015
Evolving patient selection and clinical benefit criteria for sapropterin dihydrochloride (Kuvan®) treatment of PKU patients.
Journal: Molecular genetics and metabolism
Published: November 14, 2011
Showing 1-8 of 8
Last Updated: 09/26/2026