No abstract available
MeSH terms
-
Child, Preschool
-
Craniofacial Dysostosis / diagnosis
-
Craniofacial Dysostosis / genetics*
-
Craniofacial Dysostosis / physiopathology
-
Diagnosis, Differential
-
Female
-
High-Throughput Nucleotide Sequencing
-
Humans
-
Infant
-
Karyotype
-
Micrognathism / diagnosis
-
Micrognathism / genetics*
-
Micrognathism / physiopathology
-
Mutation
-
Proteins / genetics*
Substances
-
MAGEL2 protein, human
-
Proteins