Lauren B. Carter
Pediatrics | Medical Genetics
1001 Blythe Blvd.
Suite 200
Charlotte, NC 28203
Suite 200
Charlotte, NC 28203
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 6 publications
Improving genetic testing utilization in a tertiary care neonatal intensive care unit through quality improvement.
Journal: American journal of medical genetics. Part A
Published: May 13, 2024
Unusual Dermatologic Findings in an Extremely Low Birthweight Infant: The Genetic Diagnosis.
Journal: NeoReviews
Published: September 25, 2023
Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 28, 2023
A rare cause of infantile achalasia: GMPPA-congenital disorder of glycosylation with two novel compound heterozygous variants.
Journal: American journal of medical genetics. Part A
Published: February 03, 2022
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females.
Journal: American journal of human genetics
Published: December 07, 2020
Smokers Display Reduced Glucocorticoid Sensitivity Prior to Symptomatic Chronic Disease Development.
Smokers Display Reduced Glucocorticoid Sensitivity Prior to Symptomatic Chronic Disease Development.
Journal: Annals of behavioral medicine : a publication of the Society of Behavioral Medicine
Published: September 14, 2018
Showing 1-6 of 6
Last Updated: 09/26/2026