The Genomic Organization and the Full Coding Region of the Human PAX7 Gene

This publication has 22 references indexed in Scilit:

• Cloning and Characterization of CpG Islands of the Human Chromosome 1p36 Region
  Genomics, 1996
• Structural characterization of the FKHR gene and its rearrangement in alveolar rhabdomyosarcoma
  Human Molecular Genetics, 1995
• Genomic organization of the human PAX3 gene: DNA sequence analysis of the region disrupted in alveolar rhabdomyosarcoma
  Genomics, 1995
• Agreement among and within groups of pathologists in the classification of rhabdomyosarcoma and related childhood sarcomas. Report of an international study of four pathology classifications
  Cancer, 1994
• Fusion of a fork head domain gene to PAX3 in the solid tumour alveolar rhabdomyosarcoma
  Nature Genetics, 1993
• Analysis of the Pax-3 Gene in the Mouse Mutant Splotch
  Genomics, 1993
• Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma
  Nature Genetics, 1993
• An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome
  Nature, 1992
• splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3
  Cell, 1991
• The murine paired box gene, Pax7, is expressed specifically during the development of the nervous and muscular system
  Mechanisms of Development, 1990