INTRODUCTION TO HOVERCRAFT ANDHOVERPORTS.

Por CROSS I., O'FLAHERTY C.
Publicado em 1975

Monozygotic twins with chromosome 22q11 deletion and discordant phenotype.

Por Goodship, J, Cross, I, Scambler, P, Burn, J
Publicado em 1995

Partial trisomy 3q and the mild Cornelia de Lange syndrome phenotype.

Por Ireland, M, English, C, Cross, I, Lindsay, S, Strachan, T
Publicado em 1995

A population study of chromosome 22q11 deletions in infancy

Por Goodship, J., Cross, I., LiLing, J., Wren, C.
Publicado em 1998

A de novo translocation t(3;17)(q26.3;q23.1) in a child with Cornelia de Lange syndrome.

Por Ireland, M, English, C, Cross, I, Houlsby, W T, Burn, J
Publicado em 1991

FISH studies in a patient with sporadic aniridia and t(7;11) (q31.2;p13).

Por Crolla, J A, Cross, I, Atkey, N, Wright, M, Oley, C A
Publicado em 1996

Frequency and predictive value of 22q11 deletion

Por LILING, J., CROSS, I., BURN, J., DANIEL, C, TAWN, E, PARKER, L.
Publicado em 1999

A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation.

Por Goodship, J, Curtis, A, Cross, I, Brown, J, Emslie, J, Wolstenholme, J, Bhattacharya, S, Burn, J
Publicado em 1992

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.

Por Burn, J, Takao, A, Wilson, D, Cross, I, Momma, K, Wadey, R, Scambler, P, Goodship, J
Publicado em 1993

Noonan's and DiGeorge syndromes with monosomy 22q11.

Por Wilson, D I, Britton, S B, McKeown, C, Kelly, D, Cross, I E, Strobel, S, Scambler, P J
Publicado em 1993

Alagille syndrome and deletion of 20p.

Por Anad, F, Burn, J, Matthews, D, Cross, I, Davison, B C, Mueller, R, Sands, M, Lillington, D M, Eastham, E
Publicado em 1990

An intrachromosomal insertion causing 5q22 deletion and familial adenomatous polyposis coli in two generations.

Por Cross, I, Delhanty, J, Chapman, P, Bowles, L V, Griffin, D, Wolstenholme, J, Bradburn, M, Brown, J, Wood, C, Gunn, A
Publicado em 1992

DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin.

Por Wilson, D I, Cross, I E, Goodship, J A, Coulthard, S, Carey, A H, Scambler, P J, Bain, H H, Hunter, A S, Carter, P E, Burn, J
Publicado em 1991

A prospective cytogenetic study of 36 cases of DiGeorge syndrome

Por Wilson, D. I., Cross, I. E., Goodship, J. A., Brown, J., Scambler, P. J., Bain, H. H., Taylor, J. F. N., Walsh, K., Bankier, A., Burn, J., Wolstenholme, J.
Publicado em 1992