A Search Service for Abbreviation / Long Form
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Abbreviation
:
CMT1A
Long Form
:
caused by a dominantly inherited 1.5-Mb duplication at 17p11.2-12
No.
Year
Title
Co-occurring Abbreviation
1
2002
[Molecular genetic diagnosis of Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies].
CMT
,
HNPP
,
PCR
,
PMP22
2
2001
Molecular genetic analysis of Charcot-Marie-Tooth 1A duplication in Norwegian patients by quantitative photostimulated luminescence imaging.
CMT1
,
PSL