论文信息 - Identification of Intragenic Exon Deletions and Duplication of TCF12 by Whole Genome or Targeted Sequencing as a Cause of TCF12‐Related Craniosynostosis - 字舞流文

Identification of Intragenic Exon Deletions and Duplication of TCF12 by Whole Genome or Targeted Sequencing as a Cause of TCF12‐Related Craniosynostosis

S. Knight | A. V. D. van den Ouweland | S. Twigg | A. Wilkie | P. J. van der Spek | S. McGowan | J. Goos | I. Mathijssen | A. Fenwick | S. Wall | M. V. van Dooren | A. Hoogeboom | S. Swagemakers | Frank J Magielsen | Frank J. Magielsen