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Chromosoma|January 1, 1975
Karyotype and chromosomal banding pattern in Heteropeza pygmaeaJ Fantes, R CamenzindCytogenetics and Cell Genetics|January 1, 1988
Use of an alphoid satellite sequence to locate the X chromosome automatically, with particular reference to identification of the fragile XJ Fantes, J Gosden, J PiperHuman Molecular Genetics|December 1, 1992
Lambda CM8, a human sequence with putative centromeric function, does not map to the centromere but is present in one to two copies at 9qterN I McGill, J Fantes, H CookeDifferentiation; Research in Biological Diversity|January 1, 1983
Structure and evolution of human Y chromosome DNAH J Cooke, J Fantes, D GreenProceedings of the National Academy of Sciences of the United States of America|August 15, 1991
Functional reintroduction of human telomeres into mammalian cellsC Farr, J Fantes, P Goodfellow, et al.Cytometry|January 1, 1990
Automatic detection of fragile X chromosomes using an X centromere probeJ Piper, J Fantes, J Gosden, et al.American Journal of Human Genetics|September 1, 1993
De novo microdeletion on an inherited Robertsonian translocation chromosome: a cause for dysmorphism in the apparently balanced translocation carrierD T Bonthron, S J Smith, J Fantes, et al.Genomics|June 15, 1997
The genomic organization of the murine Pax 8 gene and characterization of its basal promoterO Okladnova, A Poleev, J Fantes, et al.Nature Genetics|March 10, 2001
Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndromeD L Guris, J Fantes, D Tara, et al.Nucleic Acids Research|November 25, 1990
The structure of a subterminal repeated sequence present on many human chromosomesS Cross, J Lindsey, J Fantes, et al.Pageof 3