Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly
- 1 January 1996
- journal article
- Published by Springer Nature in Nature Genetics
- Vol. 12 (1) , 94-96
- https://doi.org/10.1038/ng0196-94
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- How neutral are synonymous codon mutations?Nature Genetics, 1995
- Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral refluxNature Genetics, 1995
- Effect on splicing of a silent FGFR2 mutation in Crouzon syndromeNature Genetics, 1995
- PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouseHuman Molecular Genetics, 1994
- Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2Nature Genetics, 1993
- Nested expression domains of four homeobox genes in developing rostral brainNature, 1992
- The human PAX6 gene is mutated in two patients with aniridiaNature Genetics, 1992
- An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndromeNature, 1992
- Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box geneNature, 1992
- A probable case of the homozygous condition of the aniridia gene.Journal of Medical Genetics, 1980