A. Caine

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Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18, and 21 by FISH or PCR without a full karyotype: a cytogenetic risk assessment

J. Crolla, J. Waters, A. Caine, 2005, The Lancet.

Counselling implications of chromosomal abnormalities other than trisomy 21 detected through a maternal serum screening programme

G. Mason, J. Williams, A. Caine, 1997, British journal of obstetrics and gynaecology.

Genetic evidence that a Y-linked gene in man is homologous to a gene on the X chromosome

P. Goodfellow, S. Povey, M. Ferguson-Smith, 1983, Nature.

Reproductive capacity and dominant lethal mutations in female guinea-pigs and Djungarian hamsters following X-rays or chemical mutagens.

M. Lyon, A. Caine, 1979, Mutation research.

The induction of chromosome aberrations in mouse dictyate oocytes by X-rays and chemical mutagens.

M. Lyon, A. Caine, 1977, Mutation research.

Cytogenetic studies in Papaver L.; the x= 6 and x= 7 diploids

A. Caine, J. Gill, 1988 .

Duplication of distal 17q from a maternal translocation: an additional case with some unique features.

R. Mueller, D. Haigh, A. Caine, 1989, Journal of medical genetics.

An unusual tricentric X chromosome detected prenatally

A. Caine, G. Mason, H. Daly, 1993, Prenatal diagnosis.

Short-term culture and false-negative results for Down's syndrome on chorionic villus sampling

R. Lilford, G. Mason, G. Linton, 1991, The Lancet.

Prenatal diagnosis – Authors' reply

J. Crolla, E. Maltby, J. Waters, 2005, The Lancet.

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

L. Al-Gazali, R. Mueller, A. McCartney, 1990, Journal of medical genetics.

Two46,XX,t(X;Y) females withlinear skin defects and congenital microphthalmia: a new syndrome atXp22.3

R. Mueller, A. McCartney, A. Caine, 1990 .