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Nature Genetics|May 10, 2000
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2A Bolino, M Muglia, F L Conforti, et al.Nature Genetics|August 1, 1993
A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10S Lyonnet, A Bolino, A Pelet, et al.European Journal of Human Genetics : EJHG|August 10, 1999
Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus--a GISC studyV Annese, A Latiano, P Bovio, et al.European Journal of Human Genetics : EJHG|October 22, 1998
First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4qM Devoto, K Shimoya, J Caminis, et al.Genomics|February 16, 2000
Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22A Bolino, E R Levy, M Muglia, et al.Nature|February 1, 1996
A common molecular basis for three inherited kidney stone diseasesS E Lloyd, S H Pearce, S E Fisher, et al.American Journal of Human Genetics|January 23, 1999
Refinement of the chromosome 5p locus for familial calcium pyrophosphate dihydrate deposition diseaseL J Andrew, V Brancolini, L S de la Pena, et al.Molecular Psychiatry|June 24, 2009
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genesJ Elia, X Gai, H M Xie, et al.Psychiatry Research|May 30, 1997
A linkage study of schizophrenia to markers within Xp11 near the MAOB geneJ Dann, L E DeLisi, M Devoto, et al.Pageof 8