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Genome Research|January 25, 2000
A consensus linkage map of the chicken genomeM A Groenen, H H Cheng, N Bumstead, et al.Nature Genetics|September 10, 1998
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2BR Bashir, S Britton, T Strachan, et al.Immunity|September 5, 1998
Targeted disruption of the mouse Caspase 8 gene ablates cell death induction by the TNF receptors, Fas/Apo1, and DR3 and is lethal prenatallyE E Varfolomeev, M Schuchmann, V Luria, et al.Molecular Psychiatry|November 26, 2014
The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesityA M Maillard, A Ruef, F Pizzagalli, et al.Annals of Neurology|August 1, 1997
A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in TurkeyP Dinçer, F Leturcq, I Richard, et al.Nature Genetics|August 31, 2001
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathyI Eisenberg, N Avidan, T Potikha, et al.Neuromuscular Disorders : NMD|October 29, 2000
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)L V Anderson, R M Harrison, R Pogue, et al.American Journal of Human Genetics|May 1, 1997
Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical originsI Richard, L Brenguier, P Dinçer, et al.Neuromuscular Disorders : NMD|December 1, 1996
Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophiesJ S Beckmann, I Richard, O Broux, et al.American Journal of Human Genetics|May 20, 1999
Calpainopathy-a survey of mutations and polymorphismsI Richard, C Roudaut, A Saenz, et al.Pageof 22