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2. Somatic cancer genetics in the UK: real-world data from phase I of the Cancer Research UK Stratified Medicine Programme

3. Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome

4. Diffuse Cystic Lung Disease of Unexplained Cause With Coexistent Small Airway Disease

5. CHRNGgenotype–phenotype correlations in the multiple pterygium syndromes

7. Multiplex ligation-dependent probe amplification (MLPA) analysis is an effective tool for the detection of novel intragenic PLA2G6 mutations: Implications for molecular diagnosis

8. Abstract 1848: Folliculin (FLCN) sequence variants involved in Birt-Hogg-Dube syndrome

9. Abstract 1851: Investigation of the Birt-Hogg-Dubé tumour suppressor gene (FLCN) in familial and sporadic colorectal cancer

10. A new locus-specific database (LSDB) for mutations in the folliculin (FLCN) gene

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