Gordon S. Stephen

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

D A Couzin, J L Watt, Gordon S. Stephen · Journal of Medical Genetics · 1987 · 87 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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

J L Watt, I. A. Olson, A W Johnston et al. · Journal of Medical Genetics · 1985 · 84 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

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

J L Watt, Ken Ward, D A Couzin et al. · Journal of Medical Genetics · 1986 · 81 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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

J L Watt, D A Couzin, DavidJ. Lloyd et al. · Journal of Medical Genetics · 1984 · 26 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Apparent Fryns' syndrome and aneuploidy: evidence for a disturbance of the midline developmental field

John Dean, D A Couzin, Elizabeth Gray et al. · Clinical Genetics · 1991 · 22 citations

Life Sciences, Genetics, Molecular Genetics +17