Fluorescence in situ hybridization analysis is useful for the diagnosis of the carrier state of X‐linked ichthyosis
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[1] M. Ishii,et al. Complementation studies with clinical and biochemical characterizations of a new variant of multiple sulphatase deficiency , 1987, Journal of Inherited Metabolic Disease.
[2] M. Valdés-Flores,et al. Carrier identification by FISH analysis in isolated cases of X-linked ichthyosis. , 2001, American journal of medical genetics.
[3] P. Yen,et al. Molecular studies of deletions at the human steroid sulfatase locus. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[4] T. Mohandas,et al. Differential expression of steroid sulphatase locus on active and inactive human X chromosome , 1982, Nature.