“C” trigonocephaly syndrome: Clinical variability and possibility of surgical treatment
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference8 articles.
1. Further delineation of the C (trigonocephaly) syndrome
2. Opitz trigonocephaly syndrome: Report of two cases
3. Trigonocephaly: A new familial syndrome
4. Anomalies associated with partial deletion of long arm of chromosome 11
5. Craniosynostosis and syndactyly: expanding the 11q-- chromosomal deletion phenotype.
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3. Compound heterozygous mutations in theIFT140gene cause Opitz trigonocephaly C syndrome in a patient with typical features of a ciliopathy;Clinical Genetics;2017-02-16
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