J. Delhanty

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Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers

P. Abou-Sleiman, J. Harper, A. Apessos, 2001, Prenatal diagnosis.

BIOPSY OF HUMAN PREIMPLANTATION EMBRYOS AND SEXING BY DNA AMPLIFICATION

J. Delhanty, A. Handyside, E. Tuddenham, 1989, The Lancet.

Analysis of the evolution of chromosome abnormalities in human embryos from Day 3 to 5 using CGH and FISH.

J. Harper, J. Delhanty, D. Daphnis, 2007, Molecular human reproduction.

Detailed FISH analysis of day 5 human embryos reveals the mechanisms leading to mosaic aneuploidy.

J. Harper, J. Delhanty, J. Delhanty, 2005, Human reproduction.

Cytogenetic and molecular investigations of Y chromosome sequences and their role in Turner syndrome

G. Conway, J. Delhanty, C. Quilter, 1998, Annals of human genetics.

Rapid sexing of human embryos by non‐radioactive in situ hybridization: Potential for preimplantation diagnosis of X‐linked disorders

S. Malcolm, J. Delhanty, J. Delhanty, 1989, Prenatal diagnosis.

Expression of genes regulating chromosome segregation, the cell cycle and apoptosis during human preimplantation development.

N. Steuerwald, A. Thornhill, D. Wells, 2005, Human reproduction.

Meiotic and mitotic behaviour of a ring/deleted chromosome 22 in human embryos determined by preimplantation genetic diagnosis for a maternal carrier

P. Serhal, J. Delhanty, A. Mania, 2009, Molecular Cytogenetics.

Preimplantation genetics: an explanation for poor human fertility?

J. Delhanty, 2001, Annals of human genetics.

Frequent normal allele loss and maternal origin of the mutation shown by DNA homoduplex analysis in a severely affected patient with adenomatous polyposis coli

S. Gayther, J. Delhanty, M. Rees, 1994, Annals of human genetics.

Molecular genetic evidence for the delineation of more severe form of familial adenomatous polyposis which results from fresh mutation

I. Talbot, J. Delhanty, S. Leigh, 1993, Annals of human genetics.

First application of preimplantation genetic diagnosis to neurofibromatosis type 2 (NF2)

P. Abou-Sleiman, J. Harper, A. Apessos, 2002, Prenatal diagnosis.

Chromosome breakage in lymphocytes from members of cancer families showing autosomal dominant inheritance

J. Delhanty, K. Tsioupra, M. N. Khouzam, 1990, Clinical Genetics.

Preimplantation genetic diagnosis

J. Harper, J. Delhanty, J. Delhanty, 2000, Current opinion in obstetrics & gynecology.

A comparison of the cytogenetic response to asbestos and glass fibre in Chinese hamster and human cell lines. Demonstration of growth inhibition in primary human fibroblasts.

J. Delhanty, A. Sincock, G Casey, 1982, Mutation research.

Loss of constitutional heterozygosity on chromosome 5q in hepatocellular carcinoma without cirrhosis.

J. Dooley, N. Habib, J. Delhanty, 1991, British Journal of Cancer.

EXPRESSION OF Xg AND THE 12E7 ANTIGEN IN PRIMATES

P. Goodfellow, J. Delhanty, P. Tippett, 1985, Journal of immunogenetics.