Nature Genetics
9, 101 - 103 (1995)
doi:10.1038/ng0295-101
Craniofacial syndromes: no such thing as a single gene diseaseJohn J. Mulvihill1
1Department of Human Genetics, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, USA REFERENCES
- Wilkie, A.O.M. et al. Nature Genet. 9, 165−172 (1995). | Article | PubMed | ISI | ChemPort |
- Rutland, P. et al. Nature Genet. 9, 173−176 (1995). | Article | PubMed | ISI | ChemPort |
- Lajeunie, E. et al. Nature Genet. 9, 108−110 (1995). | Article | PubMed | ISI | ChemPort |
- Cohen, Jr. M.M. ed. Craniosynostosis: Diagnosis, Evaluation, and Management. (Raven Press, New York, 1986).
- McKusick, V.A. Mendelian Inheritance in Man. 11th edn (Johns Hopkins University Press, Baltimore, 1994).
- Goodman, R.M. & Gortin, R.J., Malformed Infant and Child: An Illustrated Guide (Oxford University Press, New York, 1983).
- Shiang, R. et al. Cell 78, 335−342 (1994). | Article | PubMed | ISI | ChemPort |
- Rousseau, F. et al. Nature 371, 252−254 (1994). | Article | PubMed | ISI | ChemPort |
- Francomano, C.A. Entry 134934 in McKusick, V.A. Online Mendelian Inheritance in Man (Johns Hopkins University, 1995).
- Superti-Furga, A. et al. Eur. J. Pediatr. (in the press).
- Reardon, W. et al. Nature Genet. 8, 98−103 (1994). | Article | PubMed | ISI | ChemPort |
- Jabs, E.W. et al. Nature Genet. 8, 275−279 (1994). | Article | PubMed | ISI | ChemPort |
- Jackson, C.E., Weiss, L., Reynolds, W.A., Forman, T.F. & Peterson, J.A. J. Pediatr. 88, 963−968 (1976). | PubMed | ISI | ChemPort |
- Muenke, M. et al. Nature Genet. 8, 269−274 (1994). | Article | PubMed | ISI | ChemPort |
- Smith, D.W. J. Pediatr. 69, 1150−1169 (1966). | PubMed | ISI | ChemPort |
- Aase, J.M. Diagnostic dysmorphology (Plenum Medical Book, New York, 1990).
- Jones, K.L. Smith's Recognizable Patterns of Human Malformation. 4th edn (W.B. Saunders, Philadelphia, 1988).
- Kaler, S.G., Bixler, D. & Yu, P. J. Craniofac. Genet. Dev. Biol. 2, 205−213 (1982). | PubMed | ISI | ChemPort |
- Cohen, M.M. & Kreiborg, S. Am. J. med. Genet. 47, 624−632 (1993). | PubMed | ISI |
- Powars, D. & Hiti, A. Am. J. dis. Child. 147, 1197−1202 (1993). | PubMed | ISI | ChemPort |
- Easton, D.F., Ponder, M.A., Huson, S.M. & Ponder, B.A.J. Am. J. hum. Genet. 53, 305−313 (1993). | PubMed | ISI | ChemPort |
- Welsh, M.J., Tsui, L.-C., Boat, T.F. & Beaudet, A.L. in The Metabolic and Molecular Bases of Inherited Disease. 7th edn (eds Scriver, C.R., Beaudet, A.L., Sly, W.S. & Valle, D.) 3799−3876 (McGraw-Hill, New York, 1995).
- Davies, J.L. et al. Nature 371, 130−136 (1994). | Article | PubMed | ISI | ChemPort |
- Jonsson, J.J. & Weissman, S.M. Proc. natn. Acad. Sci. U.S.A. 92, 83−85 (1995). | ChemPort |
|