A Search Service for Abbreviation / Long Form

■ Abbreviation / Long Form : CMT1A / caused by a dominantly inherited 1.5-Mb duplication at 17p11.2-12

[Related PubMed/MEDLINE]
Total Number of Papers: 2
[Entries Per Page]
 per page
Page Control
Page: of
Abbreviation:   CMT1A  (>> Co-occurring Abbreviation)
Long Form:   caused by a dominantly inherited 1.5-Mb duplication at 17p11.2-12
 Abbreviation Variation
 Long Form Variation
 Pair(Abbreviation/Long Form) Variation
No. Year Title Co-occurring Abbreviation
2002 [Molecular genetic diagnosis of Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies]. CMT, HNPP, PCR, PMP22
2001 Molecular genetic analysis of Charcot-Marie-Tooth 1A duplication in Norwegian patients by quantitative photostimulated luminescence imaging. CMT1, PSL