Metopic and sagittal synostosis in Greig cephalopolysyndactyly syndrome: five cases with intragenic mutations or complete deletions of GLI3.
Greig cephalopolysyndactyly syndrome (GCPS) is a multiple congenital malformation characterised by limb and craniofacial anomalies, caused by heterozygous mutation or deletion of GLI3. We report four boys and a girl who were presented with trigonocephaly due to metopic synostosis, in association wit...
Main Authors: | Hurst, J, Jenkins, D, Vasudevan, P, Kirchhoff, M, Skovby, F, Rieubland, C, Gallati, S, Rittinger, O, Kroisel, P, Johnson, D, Biesecker, L, Wilkie, A |
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格式: | Journal article |
語言: | English |
出版: |
2011
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