protocols for diagnostics
skladny at rumms.uni-mannheim.de
Wed Oct 22 04:18:08 EST 1997
I am presently establishing a new lab for human genetic diagnosis. Does
anyone knows and uses simple but valid techniques for the diagnosis of
CF (cystic fibrosis), paternity testing, fragile-X, muscular dystrophy
type Duchenne/Becker, Familial Adenomatous Polyposis,
Hemoglobinopathies, Prader-Willi/ Angelman-syndrome, Myotonic dystrophy,
The literature gives a multitude of different protocols for the
diagnostics mentioned above, but I would like to know some really-good
working methods and protocols. I'd be very glad for any contact to
colleagues working in the same field.
Any help appreciated and thanx a lot.
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