Analysis of the developmental SIX6 homeobox gene in patients with anophthalmia/microphthalmia
- 15 July 2004
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics Part A
- Vol. 129A (1), 92-94
- https://doi.org/10.1002/ajmg.a.30126
Abstract
No abstract availableFunding Information
- Spanish Comision Interministerial de Ciencia y Tecnología (SAF99/0013-C01-02)
- Instituto de Salud Carlos III (C03/05)
This publication has 13 references indexed in Scilit:
- Multiple Hits during Early Embryonic Development: Digenic Diseases and HoloprosencephalyAmerican Journal of Human Genetics, 2002
- Novel mutation in sonic hedgehog in non‐syndromic colobomatous microphthalmiaAmerican Journal of Medical Genetics Part A, 2002
- Tissue-Specific Regulation of Retinal and Pituitary Precursor Cell ProliferationScience, 2002
- Genetic modifiers of vision and hearing.Human Molecular Genetics, 2002
- National study of microphthalmia, anophthalmia, and coloboma (MAC) in Scotland: investigation of genetic aetiologyJournal of Medical Genetics, 2002
- Human microphthalmia associated with mutations in the retinal homeobox gene CHX10Nature Genetics, 2000
- Genomic Cloning and Characterization of the Human Homeobox Gene SIX6 Reveals a Cluster of SIX Genes in Chromosome 14 and Associates SIX6 Hemizygosity with Bilateral Anophthalmia and Pituitary AnomaliesGenomics, 1999
- HOMEODOMAIN PROTEINSAnnual Review of Biochemistry, 1994
- DNA binding specificity of homeodomainsBiochemistry, 1991
- Deletion 14q (q22q23) associated with anophthalmia, absent pituitary, and other abnormalities.Journal of Medical Genetics, 1991