D. Couzin

发表

Chromosome 22q11 microdeletion and congenital heart disease – a survey in a paediatric population

J. Dean, D. Yong, P. Booth, 1999, European Journal of Pediatrics.

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

I. Auchterlonie, J. Watt, D. Couzin, 1983, Journal of medical genetics.

Variation in chiasma frequency during tulip anther development

D. Couzin, D. P. Fox, 1974, Chromosoma.

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

K. Ward, J. Watt, G. Stephen, 1986, Journal of medical genetics.

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

J. Watt, G. Stephen, D. Couzin, 1987, Journal of medical genetics.

Plating efficiency measurements and the experimental control of ageing of adult human skin fibroblasts in vitro.

D. Couzin, 1978, Experimental cell research.

CYSTIC FIBROSIS AND CHROMOSOMAL ABNORMALITIES

D. Couzin, G. Russell, D. K. Symon, 1984, The Lancet.

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

N. Haites, J. Watt, D. Couzin, 1986, Journal of medical genetics.

De novo translocation heterozygote with three reciprocal translocations.

D. Shawe, J. Watt, D. Couzin, 1983, Journal of medical genetics.

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

J. Watt, D. Couzin, E. Gray, 1981, Journal of medical genetics.

Trends in prenatal diagnosis of Down syndrome and other autosomal trisomies in Scotland 1990 to 1994, with associated cytogenetic and epidemiological findings

A. Carothers, G. Lowther, P. M. Ellis, 1999, Genetic epidemiology.

Mosaicism for a tandem duplication dup(1)(q12q22) in an 18 year old female.

J. Dean, J. Drummond, D. D. de Silva, 1998, Journal of medical genetics.

The over-dispersion between cells of chromosomal aberrations.

D. Papworth, D. Couzin, 1979, Journal of theoretical biology.

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

J. Dean, G. Stephen, D. Couzin, 1991, Clinical genetics.

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

J. Watt, G. Stephen, D. Couzin, 1985, Journal of medical genetics.

A fertile woman with non‐mosaic Turner's syndrome. Case report and review of the literature

G. Swapp, J. Watt, G. Stephen, 1989, British journal of obstetrics and gynaecology.

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

E. McKay, J. Watt, G. Stephen, 1984, Journal of medical genetics.

Interstitial deletion of chromosome 13: prognosis and adult phenotype.

J. Dean, G. Stephen, D. Couzin, 1991, Journal of medical genetics.

Frequency changes with time in vivo of radiation-induced chromosomal aberrations in skin fibroblasts.

D. Couzin, 1979, Mutation research.

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

J. Watt, D. Couzin, V. Jandial, 2022 .

A possible case of chronic leukoerythroblastosis associated with t(12;14)(p13;q22) in bone marrow cells.

A. Dawson, G. Stephen, D. Couzin, 1986, Cancer Genetics and Cytogenetics.

The prenatal detection of a familial pericentric inversion of chromosome 19

J. Watt, G. Stephen, D. Couzin, 1986, Prenatal diagnosis.