Discussion
- 1 February 1997
- journal article
- Published by Wolters Kluwer Health in Plastic and Reconstructive Surgery
- Vol. 99 (2) , 310-316
- https://doi.org/10.1097/00006534-199702000-00003
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Craniosynostoses: Phenotypic/molecular correlationsAmerican Journal of Medical Genetics, 1995
- Correction: Corrigendum: Jackson–Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2Nature Genetics, 1995
- Effect on splicing of a silent FGFR2 mutation in Crouzon syndromeNature Genetics, 1995
- Craniofacial syndromes: no such thing as a single gene diseaseNature Genetics, 1995
- Sutural biology and the correlates of craniosynostosisAmerican Journal of Medical Genetics, 1993
- Assignment of a gene locus involved in craniosynostosis to chromosome 5qterHuman Molecular Genetics, 1993
- The mapping of a gene for craniosynostosis: evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome 7p.Journal of Medical Genetics, 1992
- Birth prevalence studies of the Crouzon syndrome: comparison of direct and indirect methodsClinical Genetics, 1992
- GLI3 zinc-finger gene interrupted by translocations in Greig syndrome familiesNature, 1991