J. Ford

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The gene encoding human glutathione synthetase (GSS) maps to the long arm of chromosome 20 at band 11.2.

G. Webb, P. Board, R. Gali, 1995, Genomics.

Preconception risk factors and SGA babies: Papilloma virus, omega 3 and fat soluble vitamin deficiencies.

J. Ford, 2011, Early human development.

PALS (pregnancy and lifestyle study): association between occupational and environmental exposure to chemicals and reproductive outcome.

J. Ford, J. Hiller, L. MacCormac, 1994, Mutation research.

Insertional mutagenesis inducing hypomyelination in transgenic mice

A. Kaye, G. Webb, J. Ford, 1994, Journal of neuroscience research.

DUPLICATION OF 21 OR 8/21 TRANSLOCATION IN ACUTE LEUKÆMIA

S. Pittman, J. Ford, 1974 .

VACTERL with hydrocephalus: family with X-linked VACTERL-H.

J. Dahlstrom, F. Lomas, J. Ford, 1998, American journal of medical genetics.

1. Diet and nutrition in fertility: an overview including special requirements with ageing

J. Ford, 2014 .

Androgens Regulate Human Female Reproductive Ageing and Meiotic Fidelity

J. Ford, 2017 .

Reduced quality and accelerated follicle loss with female reproductive aging - does decline in theca dehydroepiandrosterone (DHEA) underlie the problem?

J. Ford, 2013, Journal of Biomedical Science.

Assignment, by in situ hybridization, of the growth arrest-specific gene, Gas-1, to mouse chromosome 13, bands B3-C2.

A. Evdokiou, G. Webb, J. Ford, 1992, Genomics.

Review: Molecular analysis of the Philadelphia chromosome

A. Dobrovic, G. Peters, J. Ford, 1991, Chromosoma.

Novel translocations in acute nonlymphocytic leukemia. Two cases involving chromosome 21, band q22.

G. Peters, J. Ford, R. Sage, 1990, Cancer genetics and cytogenetics.

Saturated fatty acid metabolism is key link between cell division, cancer, and senescence in cellular and whole organism aging

J. Ford, 2010, AGE.

Contribution of reciprocal translocations to an understanding of chromosome displacement: Inferences for studies of spatial order at metaphase

J. Ford, C. Roberts, 2004, Human Genetics.

Dermal necrosis and chromosome Iq abnormality in a man with a familial myeloproliferative disorder.

L. Cleland, J. Ford, C. Robinson, 1983, Australian and New Zealand journal of medicine.

Detection of X- and Y-bearing human spermatozoa after motile sperm isolation by swim-up.

C. Matthews, J. Ford, S. Flaherty, 1993, Fertility and sterility.

Differences in the error mechanisms affecting sex and autosomal chromosomes in women of different ages within the reproductive age group.

J. Russell, J. Ford, 1985, American journal of human genetics.

Detection of chromosome 17‐ and X‐bearing human spermatozoa using fluorescence in situ hybridization

C. Matthews, G. Webb, J. Ford, 1992, Molecular reproduction and development.

A fluorescent in situ hybridization analysis of the chromosome constitution of ejaculated sperm in a 47, XYY male

C. Matthews, G. Webb, J. Ford, 1994, Clinical genetics.

Chromosome elimination in micronuclei: a common cause of hypoploidy.

J. Ford, C. Schultz, A. Correll, 1988, American journal of human genetics.

Simultaneous detection of X‐ and Y‐bearing human sperm by double fluorescence in situ hybridization

C. Matthews, G. Webb, J. Ford, 1993, Molecular reproduction and development.

The XX male. Clinical and theoretical aspects.

C. Matthews, J. Ford, C. Kirby, 1983, Clinical reproduction and fertility.

Translocations of chromosome 12

J. Ford, 1981, Human Genetics.

A13‐Year Cytogenetic Study of Spontaneous Abortion: Clinical Applications of Testing

J. Ford, P. Thomas, Helen Z. Wilkin, 1996, The Australian & New Zealand journal of obstetrics & gynaecology.

Chromosome errors at mitotic anaphase.

J. Ford, A. Correll, 1992, Genome.

Aneuploidy in Humans

J. Ford, 1990 .

Chromosome flexion: potential for assessing the state of spindle assembly.

J. Ford, A. Correll, 1987, Mutation research.

Chromosome displacement and spindle tubule polymerization. 2. Effect of alterations of extracellular calcium on displacement parameters.

J. Ford, C. Roberts, 1984, Cytobios.

Displacement of chromosomes in mitosis: a technique for assessing differential chromosome error.

J. Ford, C. Roberts, 1983, Cytogenetics and cell genetics.

Factors affecting the displacement of human chromosomes from the metaphase plate.

J. Ford, P. Lester, 1982, Cytogenetics and cell genetics.

Aneuploidy Studies in Sperm: Post-Meiotic Selection against Aneuploid Sperm

G. Peters, G. Webb, J. Ford, 1994 .

Dual-label fluorescence in situ hybridization detection of individual chromosomes in sperm using ejaculated semen.

G. Webb, J. Ford, T. Han, 1994, Methods in molecular biology.

Does aneuploidy per se cause developmental abnormalities?

J. Ford, Judith Helen Ford, 1997, Mutation research.

Human papillomavirus infection and intrauterine growth restriction: a data-linkage study

D. Roder, Ming Li, W. Scheil, 2019, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Pregnancy and lifestyle study: the long-term use of the contraceptive pill and the risk of age-related miscarriage.

J. Ford, L. MacCormac, 1995, Human reproduction.

Diploid complete hydatidiform mole, mosaic for normally fertilized cells and androgenetic homozygous cells. Case report

G. Peters, J. Ford, W. Lew, 1986, British journal of obstetrics and gynaecology.

Chromosome abnormalities in chronic lymphocytic leukemia revealed by TPA as a mitogen.

D. Callen, J. Ford, 1983, Cancer genetics and cytogenetics.

Spindle microtubular dysfunction in mothers of Down syndrome children

J. Ford, 2004, Human Genetics.

A model for the mechanism of aneuploidy involving chromosome displacement.

J. Ford, 1985, Basic life sciences.

Assignment of the interleukin-2 receptor β chain gene (II-2rb) to band E on mouse chromosome 15

T. Taniguchi, G. Webb, J. Ford, 1992 .

The human glycine receptor beta subunit: primary structure, functional characterisation and chromosomal localisation of the human and murine genes.

P. Schofield, G. Sutherland, J. Lynch, 1996, Brain research. Molecular brain research.

A complex translocation in acute promyelocytic leukemia.

D. Callen, J. Ford, R. Sage, 1985, Cancer Genetics and Cytogenetics.

Cytogenetic basis of acute myeloid leukemia.

S. Pittman, P. Vincent, J. Ford, 1975, Journal of the National Cancer Institute.

Chromosomal variants and nondisjunction.

J. Ford, P. Lester, 1978, Cytogenetics and Cell Genetics.

Translocations involving chromosome 12

J. Ford, R. Rofe, Ruth P. Pavy, 1981, Human Genetics.

Interactions between C-bands of chromosomes 1 and 9 in recurrent reproductive loss

D. Callen, J. Ford, A. Jahnke, 1983, Human Genetics.

Unusual segregation in a family with a 11/21 translocation

J. Ford, U. Friedrich, Pernille Steensen, 1988, Clinical genetics.

Lack of correlation between conceptual karyotype and maternal response to placentation.

T. Khong, J. Ford, 1997, Reproduction, fertility, and development.

Hesx1, a homeobox gene expressed by murine embryonic stem cells, maps to mouse chromosome 14, bands A3-B.

P. Rathjen, G. Webb, J. Ford, 1993, Genomics.

Chromosome abnormalities in chronic lymphocytic leukemia

J. Ford, David F. Callem, 1984 .

Reduced quality and accelerated follicle loss with female reproductive aging - does decline in theca dehydroepiandrosterone (DHEA) underlie the problem?

J. Ford, 2013, Journal of Biomedical Science.

Protraction of anaphase B in lymphocyte mitosis with ageing: possible contribution to age-related cancer risk.

J. Ford, 2013, Mutagenesis.

Within pair differences of human chromosome 9 C-bands associated with reproductive loss

D. Callen, J. Ford, A. Jahnke, 2004, Human Genetics.