Chromosome Abnormalities and Genetic Counselling

Por Fitchett, M
Publicado em 1990

Predictability of VO2 max from submaximal cycle ergometer and bench stepping tests.

Por Fitchett, M A
Publicado em 1985

Deleted X chromosomes in patients with the fragile X syndrome.

Por Fitchett, M, Seabright, M
Publicado em 1984

Interstitial deletion of band 3q25.

Por Slavotinek, A M, Huson, S M, Fitchett, M
Publicado em 1997

Polycythaemia rubra vera and hairy cell leukaemia in the same patient: studies on the spleen

Por Mufti, GJ, Hamblin, TJ, Stevenson, FK, Fitchett, M
Publicado em 1982

Interstitial deletion of distal 13q associated with Hirschsprung's disease.

Por Lamont, M A, Fitchett, M, Dennis, N R
Publicado em 1989

Neurofibromatosis and childhood leukaemia/lymphoma: a population-based UKCCSG study.

Por Stiller, C. A., Chessells, J. M., Fitchett, M.
Publicado em 1994

Interstitial deletion of chromosome band 13q14 associated with squamous cell carcinoma.

Por Fitchett, M, Downing, R G, Hopkinson, D A, Bayley, A C
Publicado em 1984

Solid tissue culture for cytogenetic analysis: a collaborative survey for the Association of Clinical Cytogeneticists.

Por Rodgers, C S, Creasy, M R, Fitchett, M, Maliszewska, C T, Pratt, N R, Waters, J J
Publicado em 1996

Hirschsprung's disease associated with a deletion of chromosome 10 (q11.2q21.2): a further link with the neurocristopathies?

Por Fewtrell, M S, Tam, P K, Thomson, A H, Fitchett, M, Currie, J, Huson, S M, Mulligan, L M
Publicado em 1994

Detection of chromosomal 7 loss in myelodysplasia using an extremely polymorphic DNA probe.

Por Thein, S. L., Oscier, D. G., Jeffreys, A. J., Hesketh, C., Pilkington, S., Summers, C., Fitchett, M., Wainscoat, J. S.
Publicado em 1988

Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3.

Por al-Gazali, L I, Mueller, R F, Caine, A, Antoniou, A, McCartney, A, Fitchett, M, Dennis, N R
Publicado em 1990

Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements.

Por Horsley, S W, Knight, S J, Nixon, J, Huson, S, Fitchett, M, Boone, R A, Hilton-Jones, D, Flint, J, Kearney, L
Publicado em 1998

The association of Angelman's syndrome with deletions within 15q11-13.

Por Pembrey, M, Fennell, S J, van den Berghe, J, Fitchett, M, Summers, D, Butler, L, Clarke, C, Griffiths, M, Thompson, E, Super, M
Publicado em 1989

Characterization of three de novo derivative chromosomes 16 by “Reverse chromosome painting” and molecular analysis

Por Rack, K. A., Harris, P. C., MacCarthy, A. B., Boone, R., Raynham, H., McKinley, M., Fitchett, M., Towe, C. M., Rudd, P., Armour, J. A. L., Lindenbaum, R. H., Buckle, V. J.
Publicado em 1993