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Journal of Medical Genetics 1985;22:39-45; doi:10.1136/jmg.22.1.39
Copyright © 1985 by the BMJ Publishing Group Ltd.

Trigonocephaly and the Opitz C syndrome.

C Sargent, J Burn, M Baraitser, M E Pembrey

We present 12 cases of trigonocephaly of which six were associated with other malformations. On the basis of this experience we examine the diagnostic criteria for the presumed autosomal recessive trigonocephaly C syndrome.


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This article has been cited by other articles:

  • Yatsenko, S A, Cheung, S W, Scott, D A, Nowaczyk, M J M, Tarnopolsky, M, Naidu, S, Bibat, G, Patel, A, Leroy, J G, Scaglia, F, Stankiewicz, P, Lupski, J R (2005). Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly. J. Med. Genet. 42: 328-335 [Full Text]  

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