Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Mental Retardation and NF1[original query] |
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Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation. Neurogenetics 2006 Mar 7 (1): 59-66. Venturin Marco, Moncini Silvia, Villa Valentina, Russo Silvia, Bonati Maria Teresa, Larizza Lidia, Riva Pao |
Clinical characterisation of 29 neurofibromatosis type-1 patients with molecularly ascertained 1.4 Mb type-1 NF1 deletions. Journal of medical genetics 2010 Sep 47 (9): 623-30. Mautner V-F, Kluwe L, Friedrich R E, Roehl A C, Bammert S, Högel J, Spöri H, Cooper D N, Kehrer-Sawatzki |
A functional tetranucleotide (AAAT) polymorphism in an Alu element in the NF1 gene is associated with mental retardation. Neuroscience letters 2011 Mar 491 (2): 118-21. Védrine Sylviane Marouillat, Vourc'h Patrick, Tabagh Refaat, Mignon Laurence, Höfflin Saskya, Cherpi-Antar Catherine, Mbarek Olivier, Paubel Agathe, Moraine Claude, Raynaud Martine, Andres Christian |
Probe-based quantitative PCR assay for detecting constitutional and somatic deletions in the NF1 gene: application to genetic testing and tumor analysis. Clinical chemistry 2013 Feb . Terribas E, Garcia-Linares C, Lázaro C, Serra E |
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