J. Gosden

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The identification of human chromosomes by quinacrine fluorescence after hybridisation in situ

S. Lawrie, J. Gosden, 1980, Human Genetics.

The distribution of sequences complementary to human satellite DNAs I, II and IV in the chromosomes of chimpanzee (Pan troglodytes), gorilla (Gorilla gorilla) and orang utan (Pongo pygmaeus)

H. Seuánez, J. Gosden, C. Gosden, 1977, Chromosoma.

YAC mapping by FISH using Alu-PCR-generated probes.

D. Porteous, B. Arveiler, J. Gosden, 1992, Genomics.

Localization of the human oestrogen receptor gene to chromosome 6q24----q27 by in situ hybridization.

J. Gosden, P. Middleton, D. Rout, 1986, Cytogenetics and cell genetics.

Gene mapping and physical arrangements of human chromatin in transformed, hybrid cells: Fluorescent and autoradiographic in situ hybridization compared

D. Porteous, P. Ambros, J. Gosden, 1986, Somatic cell and molecular genetics.

A fission yeast chromosome can replicate autonomously in mouse cells

R. Allshire, P. Fantes, J. Gosden, 1987, Cell.

Localisation of a male-specific DNA fragment to a sub-region of the human Y chromosome

C. Bostock, J. Gosden, A. Mitchell, 1978, Nature.

The use of cloned Y chromosome-specific DNA probes for fetal sex determination in first trimester prenatal diagnosis

S. Christie, H. Cooke, J. Gosden, 2004, Human Genetics.

RAPID FETAL SEX DETERMINATION IN FIRST TRIMESTER PRENATAL DIAGNOSIS BY DOT HYBRIDISATION OF DNA PROBES

C. Rodeck, S. Christie, J. Gosden, 1984, The Lancet.

Restriction fragment length polymorphism analysis and assignment of the metalloproteinases stromelysin and collagenase to the long arm of chromosome 11.

D. Porteous, N. Spurr, J. Gosden, 1988, Genomics.

Telomeric repeat from T. thermophila cross hybridizes with human telomeres

S. Cross, J. Szostak, R. Allshire, 1988, Nature.

A cloned sequence, p82H, of the alphoid repeated DNA family found at the centromeres of all human chromosomes

D. Miller, J. Gosden, A. Mitchell, 2004, Chromosoma.

FIRST TRIMESTER FETAL SEXING IN PREGNANCY AT RISK FOR DUCHENNE MUSCULAR DYSTROPHY

P. Harper, J. Gosden, N. Thomas, 1983, The Lancet.

A cloned repeated DNA sequence in human chromosome heteromorphisms.

H. Cooke, S. Lawrie, J. Gosden, 1981, Cytogenetics and cell genetics.

HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.

D. Porteous, W. Bickmore, S. Christie, 1987, Proceedings of the National Academy of Sciences of the United States of America.

HRAS1-selected, chromosome mediated gene transfer; in situ hybridization with combined biotin and tritium label localizes the oncogene and reveals duplications of the human transgenome.

D. Porteous, J. Gosden, 1987, Cytogenetics and cell genetics.

The location of four human satellite DNAs on human chromosomes.

R. P. Clayton, H. Evans, R. Buckland, 1975, Experimental cell research.

Ribosomal and human-homologous repeated DNA distribution in the orangutan (Pongo pygmaeus). Comparison with distribution of these DNAs in the other species of the Hominidae.

H. Seuánez, S. Lawrie, J. Gosden, 1978, Cytogenetics and cell genetics.

Human cytochrome P-450 PB-1: a multigene family involved in mephenytoin and steroid oxidations that maps to chromosome 10.

N. Hastie, R. Meehan, N. Spurr, 1988, American journal of human genetics.

Biological properties of a tumour cell line (NB1-G) derived from human neuroblastoma.

G. Spowart, J. Gosden, R. Carachi, 1987, British Journal of Cancer.

Oligonucleotide-primed in situ DNA synthesis (PRINS): a method for chromosome mapping, banding, and investigation of sequence organization.

D. Porteous, J. Gosden, J. Fantes, 1991, Cytogenetics and cell genetics.

Chromosomal localization of the human oncogene ERBA2.

J. Gosden, P. Middleton, D. Rout, 1986, Cytogenetics and cell genetics.

Chromosomal organization of the cytochrome P450-2C gene family in the mouse: a locus associated with constitutive aryl hydrocarbon hydroxylase.

B. Taylor, R. Meehan, J. Hutton, 1988, Proceedings of the National Academy of Sciences of the United States of America.

Deleted Yq in the sterile son of a man with a satellited Y chromosome (Yqs).

G. Spowart, J. Gosden, A. Chandley, 1989, Journal of medical genetics.

Satellite DNA sequences in the human acrocentric chromosomes: information from translocations and heteromorphisms.

S. Lawrie, J. Gosden, C. Gosden, 1981, American journal of human genetics.

Further evidence consistent with Yqh as an indicator of risk of gonadal blastoma in Y‐bearing mosaic Turner syndrome

J. Gosden, P. Humphries, C. Costigan, 1992, Clinical genetics.

Mechanism of endonuclease banding of chromosomes.

N. Hastie, D. Miller, H. Evans, 1984, Experimental cell research.

The fate of DNA statellites I, II, III and ribosomal DNA in a familial dicentric chromosome 13:14

S. Lawrie, J. Gosden, C. Gosden, 1978, Human Genetics.

Satellite DNA and cytological staining patterns in heterochromatic inversions of human chromosome 9

G. Spowart, S. Lawrie, J. Gosden, 1981, Human Genetics.

Deleted Yqinthesterile sonofa man withasatellited Y chromosome (Yqs)

G. Spowart, J. Gosden, A. Chandley, 1989 .

Satellite DNA loss and nucleolar organiser activity in an individual with a de novo chromosome 13,14 translocation

S. Lawrie, J. Gosden, C. Gosden, 1979, Clinical genetics.

SV40 virus-specific RNA synthesis in transformed human cells.

J. Gosden, J. Rogers, D. Young, 1973, Nature: New biology.

Location of human satellite DNAs on the Y chromosome

H. Evans, R. Buckland, J. Gosden, 1974, Nature.

DIRECT VISION CHORION BIOPSY AND CHROMOSOME-SPECIFIC DNA PROBES FOR DETERMINATION OF FETAL SEX IN FIRST-TRIMESTER PRENATAL DIAGNOSIS

C. Rodeck, J. Gosden, C. Gosden, 1982, The Lancet.

Estimation of aneuploidy levels in human spermatozoa using chromosome specific probes and in situ hybridisation

J. Gosden, A. Chandley, A. M. Joseph, 2004, Human Genetics.

FETAL ABNORMALITIES IN CYSTIC FIBROSIS SUGGEST A DEFICIENCY IN PROTEOLYSIS OF CHOLECYSTOKININ

J. Gosden, C. Gosden, 1984, The Lancet.

A SINGLE-OPERATOR TECHNIQUE FOR FIRST-TRIMESTER CHORION BIOPSY

K. Nicolaides, C. Rodeck, J. Gosden, 1983, The Lancet.

Familial reciprocal translocation t(9;13)(p11;p12) investigated by silver staining and in situ hybridisation

J. Varley, J. Gosden, M. Hultén, 2004, Human Genetics.

Sexing the human fetus and identification of polyploid nuclei by DNA–DNA in situ hybridisation in interphase nuclei

K. Nicolaides, J. Gosden, C. Gosden, 1989, Molecular reproduction and development.

Sexing whole human pre-embryos by in-situ hybridization with a Y-chromosome specific DNA probe.

D. Baird, J. Gosden, A. Glasier, 1988, Human reproduction.

SEXING THE HUMAN PRE-EMBRYO BY DNA-DNA IN-SITU HYBRIDISATION

J. Gosden, N. Hastie, J. West, 1987, The Lancet.

Multi-PRINS: multiple sequential oligonucleotide primed in situ DNA synthesis reactions label specific chromosomes and produce bands

E. Speel, J. Gosden, A. Hopman, 2004, Human Genetics.

Multiple sequential oligonucleotide primed in situ DNA syntheses (MULTI-PRINS).

J. Gosden, D. Lawson, 1997, Methods in molecular biology.

Rapid chromosome identification by oligonucleotide-primed in situ DNA synthesis (PRINS).

J. Gosden, D. Lawson, 1994, Human molecular genetics.

PCR in situ: a rapid alternative to in situ hybridization for mapping short, low copy number sequences without isotopes.

J. Gosden, D. Hanratty, J. Gosden, 1993, BioTechniques.

Characterisation of a human Y chromosome repeated sequence and related sequences in higher primates

J. Schmidtke, H. Cooke, J. Gosden, 2004, Chromosoma.

Instant PRINS: a rapid method for chromosome identification by detecting repeated sequences in situ.

J. Gosden, D. Lawson, 1995, Cytogenetics and cell genetics.

Chromosome analysis protocols

J. Gosden, John R. Gosden, 1994 .

Identification and quantitation of human chromosomes by primedin situ synthesis

J. Gosden, 1996, Chromosome Research.

The organisation of repetitive DNA sequences on human chromosomes with respect to the kinetochore analysed using a combination of oligonucleotide primers and CREST anticentromere serum

J. Gosden, P. Jeppesen, A. Mitchell, 1992, Chromosoma.

Use of an alphoid satellite sequence to locate the X chromosome automatically, with particular reference to identification of the fragile X.

J. Piper, J. Gosden, J. Fantes, 1988, Cytogenetics and cell genetics.

Gene targeting for somatic cell manipulation: rapid analysis of reduced chromosome hybrids by Alu-PCR fingerprinting and chromosome painting.

M. Farrall, D. Porteous, J. Dorin, 1992, Human molecular genetics.

Schizophrenia-associated chromosome 11q21 translocation: identification of flanking markers and development of chromosome 11q fragment hybrids as cloning and mapping resources.

W. Muir, D. Porteous, K. Evans, 1993, American journal of human genetics.

Development of an improved technique for first‐trimester microsampling of chorion

C. Rodeck, J. Gosden, C. Gosden, 1983, British journal of obstetrics and gynaecology.

Characterisation of DNA from condensed and dispersed human chromatin.

J. Gosden, A. Mitchell, 1975, Experimental cell research.

Automatic detection of fragile X chromosomes using an X centromere probe.

J. Piper, J. Gosden, L. Ji, 1990, Cytometry.

The location of DNA homologous to human satellite III DNA in the chromosomes of chimpanzee (Pan troglodytes), gorilla (Gorilla gorilla) and orang utan (Pongo pygmaeus)

H. Seuánez, S. Lawrie, J. Gosden, 1977, Chromosoma.

Chromosomal localisation of DNA sequences in condensed and dispersed human chromatin.

R. P. Clayton, H. Evans, R. Buckland, 1975, Experimental cell research.

Characterization of a chromosome-specific chimpanzee alpha satellite subset: evolutionary relationship to subsets on human chromosomes.

J Gosden, H. Willard, P. Warburton, 1996, Genomics.

Regional localization and characterization of a DNA segment on the long arm of chromosome 21

D. Cooper, A. Goate, D. Miller, 1987, Human Genetics.

Abstracts of meeting presentations (Part 3 of 11)

A. Chapelle, J. Opitz, N. Morton, 1979 .

Satellite DNA relationships in man and the primates.

O. Ryder, J. Gosden, A. Mitchell, 1981, Nucleic acids research.

Bright-field microscopic detection of oligonucleotide PRINS-labeled DNA in chromosome preparations.

E. Speel, F. Ramaekers, J. Gosden, 1997, Methods in molecular biology.

PRINS and in situ PCR protocols

J. Gosden, 1996 .

Human interstitial retinol-binding protein (IRBP): cloning, partial sequence, and chromosomal localization

D. Ledbetter, R. Cook, S. Christie, 1987, Somatic cell and molecular genetics.

45,X/46,X dic (Y) mosaicism in a phenotypic male.

J. Gosden, P. Batstone, M. Faed, 1991, Archives of Disease in Childhood.

Abstracts of meeting presentations (Part 5 of 11)

A. Chapelle, J. Opitz, N. Morton, 1979 .

Alu- and LI-Primed PCR-Generated Probes for Nonisotopie in Situ Hybridization

J. Gosden, D. Lawson, Matthew Breen, 1994 .

Oligonucleotide Primed in Situ DNA Synthesis (PRINS)

J. Gosden, 1994 .

CHOLECYSTOKININ AND CYSTIC FIBROSIS

J. Gosden, C. Gosden, 1984, The Lancet.