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Nature Genetics|September 10, 1998
PAK3 mutation in nonsyndromic X-linked mental retardationK M Allen, J G Gleeson, S Bagrodia, et al.Genomics|August 1, 1994
Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome geneV Biancalana, E Trivier, C Weber, et al.Nature Genetics|August 1, 1992
Fragile X syndrome without CCG amplification has an FMR1 deletionA K Gedeon, E Baker, H Robinson, et al.American Journal of Medical Genetics|March 1, 1994
Hypoplasia of the cerebellar vermis and corpus callosum in thrombocytopenia with absent radius syndrome on MRI studiesM R MacDonald, G B Schaefer, A H Olney, et al.The Journal of Pediatrics|December 1, 1975
Treatment of Candida peritonitis by peritoneal lavage with amphotericin BR A Bortolussi, M R MacDonald, R M Bannatyne, et al.American Journal of Medical Genetics|February 1, 1993
Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28L C Adès, A K Gedeon, M J Wilson, et al.American Journal of Human Genetics|May 1, 1985
Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3L M Mulligan, M A Phillips, C J Forster-Gibson, et al.The Journal of Otolaryngology|June 1, 1994
Ototoxicity of carboplatin: comparing animal and clinical models at the Hospital for Sick ChildrenM R Macdonald, R V Harrison, M Wake, et al.Journal of Virology|April 10, 1999
Spliced mRNA encoding the murine cytomegalovirus chemokine homolog predicts a beta chemokine of novel structureM R MacDonald, M W Burney, S B Resnick, et al.Cancer Research|August 1, 1981
Effect of 5''-methylthioadenosine and its analogs on murine lymphoid cell proliferationR W Wolford, M R MacDonald, B Zehfus, et al.Pageof 8