De novo translocation heterozygote with three reciprocal translocations.

Por Watt, J L, Couzin, D A
Publicado em 1983

Structural rearrangements in the parents of children with primary trisomy 21.

Por Couzin, D A, Watt, J L, Stephen, G S
Publicado em 1987

Interstitial deletion of chromosome 13: prognosis and adult phenotype.

Por Dean, J C, Simpson, S, Couzin, D A, Stephen, G S
Publicado em 1991

A complex double translocation involving four chromosomes and five breakpoints in a child with mild mental retardation.

Por Couzin, D A, Watt, J L, Auchterlonie, I A
Publicado em 1983

Partial trisomy 7 (q32----qter) syndrome in two children.

Por Couzin, D A, Haites, N, Watt, J L, Johnston, A W
Publicado em 1986

A paracentric inversion of 7q illustrating a possible interchromosomal effect.

Por Watt, J L, Ward, K, Couzin, D A, Stephen, G S, Hill, A
Publicado em 1986

Prenatal detection of Turner's syndrome in conjunction with trisomy 20 mosaicism (45,X/46, X, +0).

Por Watt, J L, Couzin, D A, Johnston, A W, Jandial, V, Gray, E S
Publicado em 1981

A familial insertion involving an active nucleolar organiser within chromosome 12.

Por Watt, J L, Couzin, D A, Lloyd, D J, Stephen, G S, McKay, E
Publicado em 1984

A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome.

Por Watt, J L, Olson, I A, Johnston, A W, Ross, H S, Couzin, D A, Stephen, G S
Publicado em 1985