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Human Genetics|April 1, 1991
Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutationsN Archidiacono, M Lerone, M Rocchi, et al.
Human Genetics|January 1, 1990
A normal male with an inherited deletion of one exon within the DMD geneM Nordenskjöld, L Nicholson, L Edström, et al.
American Journal of Human Genetics|March 3, 1999
Autosomal dominant myopathy with proximal weakness and early respiratory muscle involvement maps to chromosome 2qP Nicolao, F Xiang, L G Gunnarsson, et al.
American Journal of Medical Genetics|January 24, 1998
Reactions to predictive testing in Huntington disease: case reports of coping with a new genetic statusT B Wahlin, A Lundin, L Bäckman, et al.
The Journal of General Virology|December 1, 1991
B cell phenotype-dependent expression of the Epstein-Barr virus nuclear antigens EBNA-2 to EBNA-6: studies with somatic cell hybridsB A Contreras-Brodin, M Anvret, S Imreh, et al.
Urological Research|March 26, 1999
Screening for mutations in candidate genes for hypospadiasA Nordenskjöld, E Friedman, M Tapper-Persson, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|November 1, 1991
Evaluation of DNA-based diagnosis for haemophilia AC Wadelius, M Blombäck, P Goonewardena, et al.
Human Mutation|April 24, 2001
Identification of four novel polymorphisms in the calcitonin/alpha-CGRP (CALCA) gene and an investigation of their possible associations with Parkinson disease, schizophrenia, and manic depressionS Buervenich, F Xiang, O Sydow, et al.
The Journal of Biological Chemistry|April 5, 2000
Independent regulation of the myotonic dystrophy 1 locus genes postnatally and during adult skeletal muscle regenerationM Eriksson, T Ansved, L Edstrom, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|November 1, 1993
Genetic carrier detection in Norwegian families with acute intermittent porphyriaE Sagen, A Laegreid, M Anvret, et al.
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