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Annales De Genetique|January 1, 1990
An expanded mouse-human hybrid cell panel for mapping human chromosome 16D F Callen, E Baker, H J Eyre, et al.Genomics|June 6, 1998
Localization of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosityG Kremmidiotis, E Baker, J Crawford, et al.The Journal of Investigative Dermatology|November 1, 1992
Mapping of the trichohyalin gene: co-localization with the profilaggrin, involucrin, and loricrin genesM J Fietz, G E Rogers, H J Eyre, et al.Annales De Genetique|January 1, 1990
Reassessment of two apparent deletions of chromosome 16p to an ins(11;16) and a t(1;16) by chromosome paintingD F Callen, E Baker, H J Eyre, et al.Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|April 1, 1997
Rapid detection of euchromatin by Alu-PRINS: use in clinical cytogeneticsD F Callen, M Y Yip, H J EyreClinical Genetics|February 1, 1990
A dicentric variant of chromosome 6: characterization by use of in situ hybridisation with the biotinylated probe p308D F Callen, H J Eyre, M L RingenbergsAmerican Journal of Human Genetics|September 1, 1990
The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridizationD F Callen, C J Freemantle, M L Ringenbergs, et al.Journal of Medical Genetics|July 1, 1991
A rare heteromorphism of chromosome 20 and reproductive lossD R Romain, S Whyte, D F Callen, et al.Cytogenetics and Cell Genetics|January 1, 1994
Assignment of the human skeletal muscle alpha actin gene (ACTA1) to 1q42 by fluorescence in situ hybridisationP A Akkari, H J Eyre, S D Wilton, et al.Clinical Genetics|December 1, 1990
Re-evaluation of GM2346 from a del(16)(q22) to t(4;16)(q35;q22.1)D F Callen, E G Baker, S A LanePageof 264