Judith A. Fantes

Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome

Deborah L. Guris, Judith A. Fantes, David Tara et al. · Nature Genetics · 2001 · 305 citations

Human 22Q11.2, Neurodegenerative Diseases, Molecular Neuroscience +11

Functional reintroduction of human telomeres into mammalian cells.

Christine J. Farr, Judith A. Fantes, Peter N. Goodfellow et al. · Proceedings of the National Academy of Sciences · 1991 · 188 citations · Full text

Cytogenetics, Genetics, Human Telomeres +17

The structure of a subterminal repeated sequence present on many human chromosomes

Sally H. Cross, Janet C. Lindsey, Judith A. Fantes et al. · Nucleic Acids Research · 1990 · 100 citations · Full text

Sequence Present, Dna, Genetics +22

Hardware and software requirements for quantitative analysis of comparative genomic hybridization

Stanislas du Manoir, Olli Kallioniemi, Peter Lichter et al. · Cytometry · 1995 · 83 citations · Full text

FISH Mapping of De Novo Apparently Balanced Chromosome Rearrangements Identifies Characteristics Associated with Phenotypic Abnormality

Judith A. Fantes, Elena Boland, Jacqueline Ramsay et al. · The American Journal of Human Genetics · 2008 · 81 citations · Full text

Biology, Phenotypic Abnormality, Cytogenetics +12