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Left–right asymmetrical brain function underlies much of human cognition, behavior and emotion. Abnormalities of cerebral… Expand DYX3, a locus for dyslexia, resides on chromosome 2p11-p15. We have refined its location on 2p12 to a 157 kb region in two rounds… Expand Background: Dissecting complex diseases in underlying distinct traits and studying these for their genetic basis might enhance… Expand The purpose of this study was to assess 65 pedigrees ascertained through a Bipolar I (BPI) proband for evidence of linkage, using… Expand A locus on chromosome 2p12-16 has been implicated in dyslexia susceptibility by two independent linkage studies, including our… Expand Wolcott-Rallison syndrome (WRS) is a rare, autosomal recessive disorder characterized by permanent neonatal or early infancy… Expand Epidemiological studies have shown that genetic factors contribute to the etiology of the common and serious pregnancy-specific… Expand Chromosomal translocations leading to deregulation of specific oncogenes characterize approximately 50% of cases of diffuse large… Expand Article abstract-Miyoshi myopathy (MM) is a young-adult-onset, autosomal recessive distal muscular dystrophy initially affecting… Expand Burkitt's-type lymphomas–leukaemias (BL) are monoclonal proliferations of malignant B lymphocytes1. Irrespective of whether they… Expand