Associated Papers
Exome Sequencing Studies in Syndromic Patients With Cleft Lip and/or Palate: Systematic Review.
Cárdenas-Nieto D et al.
The Cleft Palate-craniofacial Journal : Official Publication of the American Cleft Palate-craniofacial Association, 2025
Genetic analysis of a child with SATB2‑associated syndrome and literature study.
Liu Q et al.
Experimental and Therapeutic Medicine, 2023
Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome.
Zarate YA et al.
Clinical Genetics, 2017
A de novo SATB2 mutation in monozygotic twins with cleft palate, dental anomalies, and developmental delay.
Schwartz E et al.
American Journal of Medical Genetics. Part A, 2017
SATB2-associated syndrome: Mechanisms, phenotype, and practical recommendations.
Zarate YA et al.
American Journal of Medical Genetics. Part A, 2017
Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing.
Zarate YA et al.
American Journal of Medical Genetics. Part A, 2015
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