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Seminars in Cancer Biology|December 1, 1993
Acute promyelocytic leukaemia and the t(15;17) translocationE F Gillard, E SolomonNucleic Acids Research|May 26, 1987
Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency)E F Gillard, N A Affara, J R Yates, et al.Human Genetics|October 1, 1988
Linkage analysis in X-linked ichthyosis (steroid sulfatase deficiency)B Wirth, F H Herrmann, M Neugebauer, et al.Archives of Dermatological Research|January 1, 1989
Gene diagnosis in X-linked ichthyosisF H Herrmann, B Wirth, K Wulff, et al.Genomics|August 1, 1992
Polymorphisms and deduced amino acid substitutions in the coding sequence of the ryanodine receptor (RYR1) gene in individuals with malignant hyperthermiaE F Gillard, K Otsu, J Fujii, et al.Human Genetics|May 1, 1988
X chromosome deletions detectable by flow cytometry in some patients with steroid sulphatase deficiency (X-linked ichthyosis)A Cooke, E F Gillard, J R Yates, et al.Genomics|April 1, 1988
A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy geneM Burmeister, A P Monaco, E F Gillard, et al.Genomics|September 1, 1987
Multipoint linkage analysis of steroid sulfatase (X-linked ichthyosis) and distal Xp markersJ R Yates, D R Goudie, E F Gillard, et al.Symposia of the Society for Experimental Biology|January 1, 1992
The role of the skeletal muscle ryanodine receptor gene in malignant hyperthermiaD H MacLennan, K Otsu, J Fujii, et al.Genomics|November 1, 1991
A substitution of cysteine for arginine 614 in the ryanodine receptor is potentially causative of human malignant hyperthermiaE F Gillard, K Otsu, J Fujii, et al.Pageof 2