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Unique Sex-Based Approach Identifies Transcriptomic Biomarkers Associated with Non-Syndromic Craniosynostosis
Author(s) -
Brendan D. Stamper,
Sarah S. Park,
Richard P. Beyer,
Theo K. Bammler,
Michael L. Cunningham
Publication year - 2012
Publication title -
gene regulation and systems biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.534
H-Index - 18
ISSN - 1177-6250
DOI - 10.4137/grsb.s9693
Subject(s) - craniosynostosis , synostosis , medicine , fibrous joint , population , sagittal suture , dysostosis , surgery , congenital disease , environmental health
The premature fusion of one cranial suture, also referred to as non-syndromic craniosynostosis, most commonly involves premature fusion of the sagittal, coronal, or metopic sutures, in that order. Population-based epidemiological studies have found that the birth prevalence of single-suture craniosynostosis is both suture- and sex-dependent.

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