Toward understanding the pathogenesis of craniosynostosis through clinical and molecular correlates
- 1 February 1998
- journal article
- review article
- Published by Wiley in Clinical Genetics
- Vol. 53 (2), 79-86
- https://doi.org/10.1111/j.1399-0004.1998.tb02648.x
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndromeNature Genetics, 1996
- Transcription factors in diseaseCurrent Opinion in Genetics & Development, 1996
- Two craniosynostotic patients with 11q deletions, and review of 48 casesAmerican Journal of Medical Genetics, 1995
- Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson—Weiss syndromeHuman Molecular Genetics, 1995
- A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasiaNature Genetics, 1995
- Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndromeNature Genetics, 1995
- Isolation of a Yeast Artificial Chromosome Contig Spanning the Greig Cephalopolysyndactyly Syndrome (GCPS) Gene RegionGenomics, 1994
- Saethre‐Chotzen syndrome with familial translocation at chromosome 7p22American Journal of Medical Genetics, 1993
- Craniosynostosis, midfacial hypoplasia, and foot abnormalities: An autosomal dominant phenotype in a large Amish kindredThe Journal of Pediatrics, 1976
- Ein Beitrag zum Turmschädelproblem, (Pathogenese, Erblichkeit und Symptomatologie)Zeitschrift für Neurologie, 1931