Functional reintroduction of human telomeres into mammalian cells.

Tekijä Farr, C, Fantes, J, Goodfellow, P, Cooke, H
Julkaistu 1991

De novo microdeletion on an inherited Robertsonian translocation chromosome: a cause for dysmorphism in the apparently balanced translocation carrier.

Tekijä Bonthron, D T, Smith, S J, Fantes, J, Gosden, C M
Julkaistu 1993

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

Tekijä Cross, S, Lindsey, J, Fantes, J, McKay, S, McGill, N, Cooke, H
Julkaistu 1990

Isolation of BAC clones spanning the Xq22.3 translocation breakpoint in a lissencephaly patient with a de novo X;2 translocation.

Tekijä Matsumoto, N, Pilz, D T, Fantes, J A, Kittikamron, K, Ledbetter, D H
Julkaistu 1998

Confirmation of CHD7 as a cause of CHARGE association identified by mapping a balanced chromosome translocation in affected monozygotic twins

Tekijä Johnson, D, Morrison, N, Grant, L, Turner, T, Fantes, J, Connor, J M, Murday, V
Julkaistu 2006

Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14

Tekijä Ungaro, P., Christian, S., Fantes, J., Mutirangura, A., Black, S., Reynolds, J., Malcolm, S., Dobyns, W., Ledbetter, D.
Julkaistu 2001

A novel atypical 22q11.2 distal deletion in father and son

Tekijä Garcia-Minaur, S, Fantes, J, Murray, R, Porteous, M, Strain, L, Burns, J, Stephen, J, Warner, J
Julkaistu 2002

Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15q

Tekijä Fantes, J, Mewborn, S, Lese, C, Hedrick, J, Brown, R, Dyomin, V, Chaganti, R, Christian, S, Ledbetter, D
Julkaistu 2002

Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization.

Tekijä Fantes, J A, Bickmore, W A, Fletcher, J M, Ballesta, F, Hanson, I M, van Heyningen, V
Julkaistu 1992

APC mutation analysis by chemical cleavage of mismatch and a protein truncation assay in familial adenomatous polyposis.

Tekijä Prosser, J., Condie, A., Wright, M., Horn, J. M., Fantes, J. A., Wyllie, A. H., Dunlop, M. G.
Julkaistu 1994

A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.

Tekijä Crolla, J A, Cawdery, J E, Oley, C A, Young, I D, Gray, J, Fantes, J, van Heyningen, V
Julkaistu 1997

Variegated transgene expression in mouse mammary gland is determined by the transgene integration locus.

Tekijä Dobie, K W, Lee, M, Fantes, J A, Graham, E, Clark, A J, Springbett, A, Lathe, R, McClenaghan, M
Julkaistu 1996

Lack of X inactivation associated with maternal X isodisomy: evidence for a counting mechanism prior to X inactivation during human embryogenesis.

Tekijä Migeon, B. R., Jeppesen, P., Torchia, B. S., Fu, S., Dunn, M. A., Axelman, J., Schmeckpeper, B. J., Fantes, J., Zori, R. T., Driscoll, D. J.
Julkaistu 1996

Molecular and physical arrangements of human DNA in HRAS1-selected, chromosome-mediated transfectants.

Tekijä Porteous, D J, Morten, J E, Cranston, G, Fletcher, J M, Mitchell, A, van Heyningen, V, Fantes, J A, Boyd, P A, Hastie, N D
Julkaistu 1986

Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome.

Tekijä van Heyningen, V, Boyd, P A, Seawright, A, Fletcher, J M, Fantes, J A, Buckton, K E, Spowart, G, Porteous, D J, Hill, R E, Newton, M S
Julkaistu 1985

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

Tekijä Fantes, J.A., Boland, E., Ramsay, J., Donnai, D., Splitt, M., Goodship, J.A., Stewart, H., Whiteford, M., Gautier, P., Harewood, L., Holloway, S., Sharkey, F., Maher, E., van Heyningen, V., Clayton-Smith, J., Fitzpatrick, D.R., Black, G.C.M.
Julkaistu 2008

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

Tekijä Fantes, J.A., Boland, E., Ramsay, J., Donnai, D., Splitt, M., Goodship, J.A., Stewart, H., Whiteford, M., Gautier, P., Harewood, L., Holloway, S., Sharkey, F., Maher, E., van Heyningen, V., Clayton-Smith, J., Fitzpatrick, D.R., Black, G.C.M.
Julkaistu 2008