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You searched for: Author/Creator Mandich, P- Mandich, P [remove] 3
- 616.8 3
- Nervous system -- Surgery -- Periodicals 3
- Neurology -- Periodicals 3
- Psychiatry -- Periodicals 3
- CMT, Charcot–Marie–Tooth disease -- HMSN, hereditary motor and sensory neuropathy -- HNPP, hereditary neuropathy with liability to pressure palsies -- P0, myelin protein zero -- SSCP, single strand conformation polymorphism 1
- CMT1A, Charcot-Marie-Tooth disease type 1A -- HNPP, hereditary neuropathy with liability to pressure palsies -- PFGE, pulsed field gel electrophoresis -- SSCP, single strand conformation polymorphism 1
- HNPP -- splice site mutation -- PMP22 1
- counselling -- predictive testing 1
- myelin protein zero -- axonal peripheral neuropathies -- Charcot-Marie-Tooth disease type 2 1