Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 30 publications
Providing Cleft Care Globally: Equity, Outcomes, and Evolving Models of Care Delivery.
Journal: Oral and maxillofacial surgery clinics of North America
Published: March 09, 2026
Partners in African Cleft Training (PACT): Evolution of a Partnership Supporting Sustainable Interdisciplinary Cleft Team Care in Sub-Saharan Africa.
Journal: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association
Published: April 14, 2025
Genetic Testing in Craniofacial Care: Development of Algorithms for Testing Patients with Orofacial Clefting, Branchial Arch Anomalies, and Craniosynostosis.
Journal: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association
Published: August 19, 2024
Isolated frontosphenoidal craniosynostosis: An argument for genetic testing.
Journal: American journal of medical genetics. Part A
Published: April 21, 2023
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice.
Journal: Science advances
Published: March 10, 2023
Dominant-negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome.
Journal: Annals of clinical and translational neurology
Published: January 30, 2023
A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature.
Journal: American journal of medical genetics. Part A
Published: November 18, 2022
Damaging variants in FOXI3 cause microtia and craniofacial microsomia.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 01, 2022
Cleft palate morphology, genetic etiology, and risk of mortality in infants with Robin sequence.
Journal: American journal of medical genetics. Part A
Published: June 02, 2021
Targeted long-read sequencing identifies missing disease-causing variation.
Journal: American journal of human genetics
Published: April 06, 2021
Reply: MN1 gene loss-of-function mutation causes cleft palate in a pedigree.
Journal: Brain : a journal of neurology
Published: December 22, 2020
Haploinsufficiency of SF3B2 causes craniofacial microsomia.
Journal: Nature communications
Published: November 12, 2020
Last Updated: 09/26/2026