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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.Genomics|September 24, 1999
Refined linkage disequilibrium and physical mapping of the gene locus for X-linked dystonia-parkinsonism (DYT3)A H Németh, D Nolte, E Dunne, et al.Human Molecular Genetics|April 18, 2000
Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pumpR Sudbrak, J Brown, C Dobson-Stone, 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.Autism Research : Official Journal of the International Society for Autism Research|March 18, 2014
A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthmaFabiola Ceroni, Angela Sagar, Nuala H Simpson, et al.Molecular Psychiatry|October 13, 2006
Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexiaD Harold, S Paracchini, T Scerri, et al.American Journal of Human Genetics|March 15, 2002
FOXP2 is not a major susceptibility gene for autism or specific language impairmentD F Newbury, E Bonora, J A Lamb, et al.American Journal of Human Genetics|August 21, 2002
Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autismSusan L Smalley, Vlad Kustanovich, Sonia L Minassian, et al.Genes, Brain, and Behavior|February 28, 2014
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairmentR Nudel, N H Simpson, G Baird, et al.Journal of Endocrinological Investigation|August 11, 2020
Testosterone treatment is associated with reduced adipose tissue dysfunction and nonalcoholic fatty liver disease in obese hypogonadal menE Maseroli, P Comeglio, C Corno, et al.Pageof 59