PRENATAL DIAGNOSIS OF X-LINKED MYOTUBULAR MYOPATHY: STRATEGIES USING NEW AND TIGHTLY LINKED DNA MARKERS
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference31 articles.
1. X-linked recessive myotubular myopathy: I. Clinical and pathologic findings in a family
2. Sporadic occurrence of Duchenne Muscular Dystrophy: evidence for new mutation
3. Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28
4. X linked myotubular myopathy (MTM1) maps between DXS304 and DXS305, closely linked to the DXS455 VNTR and a new, highly informative microsatellite marker (DXS1684).
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1. Muscle function in A canine model of X-linked myotubular myopathy;Muscle & Nerve;2012-09-13
2. Congenital myopathies/dystrophies;Neurologic Clinics;2003-11
3. The novel contiguous gene syndrome of myotubular myopathy (MTM1), male hypogenitalism and deletion in Xq28:report of the first familial case;Cytogenetic and Genome Research;1999
4. Extensive germinal mosaicism in a family with X linked myotubular myopathy simulates genetic heterogeneity.;Journal of Medical Genetics;1998-03-01
5. Confirmation of prenatal diagnosis results of X-linked recessive myotubular myopathy by mutational screening, and description of three new mutations in theMTM1 gene;Human Mutation;1998
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