The Human BARX2 Gene: Genomic Structure, Chromosomal Localization, and Single Nucleotide Polymorphisms

This publication has 14 references indexed in Scilit:

• Centre d'Etude du polymorphisme humain (CEPH): Collaborative genetic mapping of the human genome
  Published by Elsevier ,2004
• MouseOtlx2/RIEGExpression in the Odontogenic Epithelium Precedes Tooth Initiation and Requires Mesenchyme-Derived Signals for Its Maintenance
  Developmental Biology, 1997
• Barx2 , a new homeobox gene of the Bar class, is expressed in neural and craniofacial structures during development
  Proceedings of the National Academy of Sciences, 1997
• Otlx2,anOtx-Related Homeobox Gene Expressed in the Pituitary Gland and in a Restricted Pattern in the Forebrain
  Molecular and Cellular Neuroscience, 1996
• Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.
  Journal of Medical Genetics, 1996
• Mechanism of induction ofBar-like eye malformation by transient overexpression ofBar homeobox genes inDrosophila melanogaster
  Genetica, 1993
• Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4
  Nature Genetics, 1992
• Subtype determination of Drosophila embryonic external sensory organs by redundant homeo box genes BarH1 and BarH2.
  Genes & Development, 1992
• Dual Bar homeo box genes of Drosophila required in two photoreceptor cells, R1 and R6, and primary pigment cells for normal eye development.
  Genes & Development, 1992
• Partial deletion of long arm of chromosome 11[del(11)(q23)]: Jacobsen syndrome. Two new cases and review of the clinical findings.
  Journal of Medical Genetics, 1977