Fingering fibroblast growth factor receptors

This publication has 10 references indexed in Scilit:

• Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome
  Nature Genetics, 1994
• Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
  Published by Elsevier ,1994
• Two Craniosynostotic Syndrome Loci, Crouzon and Jackson-Weiss, Map to Chromosome 10q23-q26
  Genomics, 1994
• A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10
  Nature Genetics, 1994
• Localization of the achondroplasia gene to the distal 2. 5 Mb of human chromosome 4p
  Human Molecular Genetics, 1994
• A gene for achondroplasia–hypochondroplasia maps to chromosome 4p
  Nature Genetics, 1994
• The gene for achondroplasia maps to the telomeric region of chromosome 4p
  Nature Genetics, 1994
• Mutations in the α1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia
  Nature Genetics, 1993
• A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
  Cell, 1993
• Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene
  Nature, 1992