Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency
Version of Record online: 24 DEC 2001
Volume 57, Issue 5, pages 388–393, May 2000
How to Cite
Nowaczyk, M. J., Huggins, M. J., Tomkins, D. J., Rossi, E., Ramsay, J. A., Woulfe, J., Scherer, S. W. and Belloni , E. (2000), Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency. Clinical Genetics, 57: 388–393. doi: 10.1034/j.1399-0004.2000.570510.x
- Issue online: 24 DEC 2001
- Version of Record online: 24 DEC 2001
- Received 30 November 1999Accepted 20 January 2000
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