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Journal of Clinical & Laboratory Immunology|January 1, 1990
Monoclonal antibodies to chick renal calcium regulating hemeproteins. Biochemical and immunohistochemical interactions with mitochondrial 25-hydroxyvitamin D3 hydroxylasesM L Mandel, B Moorthy, S J Swartz, et al.
The Journal of Clinical Investigation|August 1, 1994
Identification of mutations in the putative ATP-binding domain of the adrenoleukodystrophy geneP Fanen, S Guidoux, C O Sarde, et al.
American Journal of Human Genetics|January 1, 1990
The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15A Hanauer, M Chery, R Fujita, et al.
Revue Neurologique|August 14, 2013
Adult centronuclear myopathies: A hospital-based studyA Echaniz-Laguna, V Biancalana, J Böhm, et al.
Annals of Emergency Medicine|February 1, 1993
Education in adult basic life support training programsL S Flint, J E Billi, K Kelly, et al.
American Journal of Human Genetics|June 1, 1996
Mutational and protein analysis of patients and heterozygous women with X-linked adrenoleukodystrophyV Feigenbaum, G Lombard-Platet, S Guidoux, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1984
Genetic mapping of the human X chromosome by using restriction fragment length polymorphismsD Drayna, K Davies, D Hartley, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1997
Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutationsM Cossée, M Schmitt, V Campuzano, et al.
American Journal of Human Genetics|February 1, 1988
Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B familiesB Arveiler, I Oberlé, A Vincent, et al.
The EMBO Journal|July 1, 1985
Extensive DNA sequence homologies between the human Y and the long arm of the X chromosomeD Geldwerth, C Bishop, G Guellaën, et al.
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