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:
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Abbreviation:
CMT1A
(
>> Co-occurring Abbreviation
)
Long Form:
caused by a dominantly inherited 1.5-Mb duplication at 17p11.2-12
Abbreviation Variation
CMT1A (2 times)
Long Form Variation
caused by a dominantly inherited 1.5-Mb duplication at 17p11.2-12 (1 time)
caused by a dominantly inherited 1.5 Mb duplication at 17p11.2-12 (1 time)
Pair(Abbreviation/Long Form) Variation
CMT1A / caused by a dominantly inherited 1.5 Mb duplication at 17p11.2-12 (1 time)
CMT1A / caused by a dominantly inherited 1.5-Mb duplication at 17p11.2-12 (1 time)
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