We have developed a method, which we have named hybridization-banding, to i
dentify simultaneously all chromosomes in a mouse metaphase spread. The met
hod uses a combination of hybridization probes labeled with a single fluor
to yield a simple, unique, readily identifiable hybridization pattern on ea
ch chromosome. The method is superior to Giemsa- or fluorescence-based band
ing methods for chromosome identification because the hybridization pattern
s are simpler and easier to identify, and unique patterns can be designed a
t will for each chromosome. Analysis can be performed with a standard fluor
escence microscope, and images call be recorded on film with an ordinary 35
-mm camera, making the method useful to many investigators. The method can
also be applied to any species for which chromosomes and probes can be prep
ared.