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Cleft Palate in Apert Syndrome
Delayna Willie
,
Greg Holmes
, Ethylin Wang Jabs
, Meng Wu
Friedman Brain Institute
Genetics and Genomic Sciences
Icahn School of Medicine at Mount Sinai
Graduate School of Biomedical Sciences
Pediatrics
Research output
:
Contribution to journal
›
Review article
›
peer-review
10
Scopus citations
Overview
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Keyphrases
Apert Syndrome
100%
Bifid Uvula
9%
Cellular Mechanisms
9%
Cleft Palate
100%
Clinical Characteristics
9%
Craniosynostosis
9%
Downstream Signaling
9%
Epithelial-mesenchymal Interaction
9%
Fibroblast Growth Factor Receptor 2 (FGFR2)
18%
Genetic Causes
9%
Hard Palate
18%
High Arched Palate
9%
Limb Anomalies
9%
Midface Retrusion
9%
Mouse Model
18%
Novel Therapeutics
9%
Palatal Defect
36%
Palatal Swelling
9%
Palate
9%
Palatogenesis
9%
Pathogenic Mechanism
18%
Rare Genetic Disease
9%
Signaling Mechanism
9%
Signaling Network
9%
Signaling Pathway
9%
Soft Palate
9%
Therapeutic Solutions
9%
Medicine and Dentistry
Apert Syndrome
100%
Cell Signaling Pathway
9%
Cellular Mechanism
9%
Cleft
9%
Cleft Palate
100%
Craniofacial Synostosis
9%
Fibroblast Growth Factor Receptor 2
18%
Genetic Disorder
9%
Hard Palate
18%
High Arched Palate
9%
Limb Malformation
9%
Palatal Swelling
9%
Palate
9%
Signaling Mechanism
9%
Soft Palate
9%
Uvula
9%
Pharmacology, Toxicology and Pharmaceutical Science
Acrocephalosyndactyly
100%
Cleft Palate
100%
Craniofacial Synostosis
9%
Fibroblast Growth Factor Receptor 2
18%
Genetic Disorder
9%
High Arched Palate
9%
Limb Malformation
9%
Mouse Model
18%