Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Myotonic Dystrophy and ZNF9[original query] |
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Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian population. Molecular and cellular probes 2005 Feb 19 (1): 71-4. Vallo L, Bonifazi E, Borgiani P, Novelli G, Botta |
Validation of sensitivity and specificity of tetraplet-primed PCR (TP-PCR) in the molecular diagnosis of myotonic dystrophy type 2 (DM2). The Journal of molecular diagnostics : JMD 2010 Sep 12 (5): 601-6. Catalli Claudio, Morgante Alessandra, Iraci Raniero, Rinaldi Fabrizio, Botta Annalisa, Novelli Giusep |
Dutch myotonic dystrophy type 2 patients and a North-African DM2 family carry the common European founder haplotype. European journal of human genetics : EJHG 2011 1 19 (5): 567-70. Coenen Marieke J H, Tieleman Alide A, Schijvenaars Mascha M V A P, Leferink Maike, Ranum Laura P W, Scheffer Hans, van Engelen Baziel G |
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