Identification and characterisation of a small marker chromosome using non-isotopic in situ hybridisation with X and Y specific probes.

समान संसाधन

• A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man.
  द्वारा: Crolla, J A, और अन्य
  प्रकाशित: (1992)
• An investigation of ring and dicentric chromosomes found in three Turner's syndrome patients using DNA analysis and in situ hybridisation with X and Y chromosome specific probes.
  द्वारा: Cooper, C, और अन्य
  प्रकाशित: (1991)
• Elucidation of structural abnormalities of the X chromosome using fluorescence in situ hybridisation with a Y chromosome painting probe.
  द्वारा: Howell, R T, और अन्य
  प्रकाशित: (1994)
• Imbalances of chromosome 17 in medulloblastomas determined by comparative genomic hybridisation and fluorescence in situ hybridisation
  द्वारा: Nicholson, J, और अन्य
  प्रकाशित: (2000)
• Identification of monosomy 3 in choroidal melanoma by chromosome in situ hybridisation
  द्वारा: Sandinha, M T, और अन्य
  प्रकाशित: (2004)