Molecular characterization of a familial translocation implicates disruption of HDAC9 and possible position effect on TGFβ2 in the pathogenesis of Peters’ anomaly
- 1 May 2003
- Vol. 81 (5) , 489-503
- https://doi.org/10.1016/s0888-7543(03)00046-6
Abstract
No abstract availableKeywords
This publication has 47 references indexed in Scilit:
- Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primerPublished by Elsevier ,2004
- Chromosomal organization and localization of the human histone deacetylase 9 gene (HDAC9)Biochemical and Biophysical Research Communications, 2002
- A Spectrum of FOXC1 Mutations Suggests Gene Dosage as a Mechanism for Developmental Defects of the Anterior Chamber of the EyeAmerican Journal of Human Genetics, 2001
- Mammalian lysophospholipasesBiochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids, 1999
- Genetics of aniridia and anterior segment dysgenesis.British Journal of Ophthalmology, 1996
- HDA1 and HDA3 Are Components of a Yeast Histone Deacetylase (HDA) ComplexPublished by Elsevier ,1996
- Anterior segment malformations in 18q-(de Grouchy) syndromeOphthalmic Paediatrics and Genetics, 1993
- Heterogeneity in dominant anterior segment malformations.British Journal of Ophthalmology, 1991
- Interstitial deletion 2q14q21American Journal of Medical Genetics, 1989
- Ocular findings in a 4 p- deletion syndrome (Wolf-Hirschhorn)Ophthalmic Paediatrics and Genetics, 1989