Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the Literature.
International Journal of Molecular Sciences（2017）
Key words
1p32p31 deletion,moyamoya syndrome,craniosynostosis,FOXD3,FOXC1,FOX genes
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