J. Delhanty

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Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disorders

C. Rodeck, P. Abou-Sleiman, J. Harper, 2002, Prenatal diagnosis.

Single cell detection of inherited retinoblastoma predisposition

J. Delhanty, M. Sütterlin, P. Sleiman, 1999, Prenatal diagnosis.

J. Harper, J. Delhanty, E. Pergament, 2004, European journal of obstetrics, gynecology, and reproductive biology.

Expression from the proximal promoter of the carbonic anhydrase 1 gene as a marker for differentiation in colon epithelia.

I. Talbot, J. Delhanty, J. Sowden, 1993, Differentiation; research in biological diversity.

Detailed chromosomal and molecular genetic analysis of single cells by whole genome amplification and comparative genomic hybridisation.

J. Delhanty, A. Handyside, J. Sherlock, 1999, Nucleic acids research.

Preimplantation genetic diagnosis for myotonic dystrophy type 1: detection of crossover between the gene and the linked marker APOC2

S. Dhanjal, J. Harper, A. Doshi, 2007, Prenatal diagnosis.

Pregnancy following preimplantation genetic diagnosis for Crouzon syndrome.

P. Abou-Sleiman, J. Harper, A. Apessos, 2002, Molecular human reproduction.

First clinical application of comparative genomic hybridization and polar body testing for preimplantation genetic diagnosis of aneuploidy.

K. Hirschhorn, B. Levy, D. Wells, 2002 .

Familial polyposis coli: no evidence for increased sensitivity to mitomycin C.

J. Attwood, J. Delhanty, H. Mazzullo, 1988, Journal of medical genetics.

Familial Raynaud's phenomenon and localized scleroderma associated with essential telangiectasia and cytogenetic abnormalities

O. P. Gray, C. Bunker, J. Delhanty, 1990, Journal of the Royal Society of Medicine.

Growth, DNA repair, sister chromatid exchange and chromosome studies in fibroblasts fromHuntington's disease patients

J. Attwood, J. Delhanty, J. Delhanty, 1981, Annals of Human Genetics.

The impact of mosaicism in preimplantation genetic diagnosis (PGD): approaches to PGD for dominant disorders in couples without family history

S. Dhanjal, A. Doshi, P. Serhal, 2016, Prenatal diagnosis.

A novel, de novo germline TP53 mutation in a rare presentation of the Li-Fraumeni syndrome in the maxilla.

P. Abou-Sleiman, J. Delhanty, A. Patrikidou, 2002, Oral oncology.

Mutations of adenomatous polyposis coli (APC) gene are uncommon in sporadic desmoid tumours.

P. Radice, M. Pierotti, S. Pilotti, 1998, British Journal of Cancer.

Somatic mutation of APC gene in desmoid tumour in familial adenomatous polyposis

J. Delhanty, J. Delhanty, R. Luijt, 1993, The Lancet.

Chromosome allele loss in colorectal liver metastases and its association with clinical features

J. Dooley, N. Habib, J. Delhanty, 1994, The British journal of surgery.

Loss of constitutional heterozygosity on chromosomes 5 and 17 in cholangiocarcinoma.

J. Dooley, N. Habib, J. Delhanty, 1993, British Journal of Cancer.

First clinical application of comparative genomic hybridization and polar body testing for preimplantation genetic diagnosis of aneuploidy.

K. Hirschhorn, B. Levy, D. Wells, 2002, Fertility and sterility.

Regionally clustered APC mutations are associated with a severe phenotype and occur at a high frequency in new mutation cases of adenomatous polyposis coli.

S. Gayther, D. Wells, J. Delhanty, 1994, Human molecular genetics.

The Origins of Aneuploidy in Human Embryos

J. Delhanty, E. Fragouli, 2013 .

Multicolour FISH detects frequent chromosomal mosaicism and chaotic division in normal preimplantation embryos from fertile patients

J. Harper, A. Ao, J. Delhanty, 1997, Human Genetics.

Preimplantation genetic diagnosis: recent triumphs and remaining challenges

J. Delhanty, S. SenGupta, 2012, Expert review of molecular diagnostics.

Germline rearrangement of MCC and APC detected by pulsed field gel electrophoresis and fluorescent in situ hybridization

S. Gayther, J. Burn, D. Wells, 1993, Annals of human genetics.

Identification of novel Asian Indian and Japanese mutations causing β-thalassaemia in the Egyptian population

J. Delhanty, M. Petrou, A. Khalifa, 1997, Human Genetics.

Prenatal detection of fetal aneuploidies using transcervical cell samples.

C. Rodeck, B. Tutschek, M. Adinolfi, 1997, Journal of medical genetics.

Deletion and duplication of the adenomatous polyposis coli gene resulting from an interchromosomal insertion involving 5(q22q23.3) in the father

J. Delhanty, R. Hastings, D. Wells, 2000, Journal of medical genetics.

Loss of heterozygosity on chromosome arms 5q, IIp, IIq, I3q, and I6p in Human Testicular Germ Cell Tumors

S. Povey, J. Delhanty, J. Parrington, 1995 .

An intrachromosomal insertion causing 5q22 deletion and familial adenomatous polyposis coli in two generations.

D. Griffin, M. Bradburn, J. Delhanty, 1992, Journal of medical genetics.

Familial Langdon Down anomaly with chromosomal fusion

L. Penrose, J. Delhanty, 1962, Annals of human genetics.

Presence of chromosomal mosaicism in abnormal preimplantation embryos detected by fluorescence in situ hybridisation

J. Harper, E. Coonen, J. Geraedts, 1994, Human Genetics.

The use of DNA from paraffin wax preserved tissue for predictive diagnosis in familial adenomatous polyposis.

J. Neoptolemos, D. Morton, J. Delhanty, 1992, Journal of medical genetics.

TheuseofDNA fromparaffin wax preserved tissue forpredictive diagnosis infamilial adenomatous polyposis

D. Morton, J. Delhanty, C. Mckeown, 1992 .

Increased susceptibility to maternal aneuploidy demonstrated by comparative genomic hybridization analysis of human MII oocytes and first polar bodies

J. Mills, D. Wells, J. Delhanty, 2006, Cytogenetic and Genome Research.

A comparative study between infertile males and patients with Turner syndrome to determine the influence of sex chromosome mosaicism and the breakpoints of structurally abnormal Y chromosomes on phenotypic sex

G. Conway, P. Serhal, J. Delhanty, 2002, Journal of medical genetics.

Use of fluorescent in situ hybridization to confirm trisomy of chromosome region 1q32‐qter as the sole karyotypic defect in a colon cancer cell line

D. Griffin, J. Delhanty, S. Leigh, 1990, Genes, chromosomes & cancer.

Familial polyposis coli: growth characteristics of karyotypically variable cultured fibroblasts, response to epidermal growth factor and the tumour promoter 12-0-tetradecanoyl phorbol-13-acetate.

M. Davis, J. Delhanty, S. Rider, 1986, Journal of medical genetics.

Human guanylate kinase (GUK1): cDNA sequence, expression and chromosomal localisation

D. Hunt, N. Katsanis, J. Fitzgibbon, 1996, FEBS letters.

Chromosome studies on 21 Przewalski horses

J. Delhanty, C. Hawkey, L. West, 1979 .

Homologies between human and marmoset (Callithrix jacchus) chromosomes revealed by comparative chromosome painting.

D. Griffin, J. Delhanty, J. Sherlock, 1996, Genomics.

Localisation of the gene encoding diacylglycerol kinase 3 (DAGK3) to human chromosome 3q27-28 and mouse chromosome 16.

M. Kai, D. Hunt, J. Fitzgibbon, 1995, Current eye research.

A technique for eliminating allele specific amplification failure during DNA amplification of heterozygous cells for preimplantation diagnosis.

J. Delhanty, N. el-Hashemite, 1997, Molecular human reproduction.

The origin of isochromosomes

J. Delhanty, J. Parrington, 1988, Clinical genetics.

Loss of heterozygosity on chromosome arms 5q, 11p, 11q, 13q, and 16p in human testicular germ cell tumors.

S. Povey, J. Delhanty, J. Parrington, 1995, Genes, chromosomes & cancer.

Original Articles the Uk Northern Region Genetic Register for Familial Adenomatous Polyposis Coli: Use of Age of Onset, Congenital Hypertrophy of the Retinal Pigment Epithelium, and Dna Markers in Risk Calculations

J. Burn, F. Lalloo, J. Delhanty, 2022 .

Different DNA changes in primary and recurrent hepatocellular carcinoma.

J. Dooley, N. Habib, J. Delhanty, 1992, Gut.

Mosaicism of autosomes and sex chromosomes in morphologically normal, monospermic preimplantation human embryos

J. Harper, E. Coonen, J. Delhanty, 1995, Prenatal diagnosis.

DNA synthesis in normal and xeroderma pigmentosum fibroblasts following treatment with 8-methoxypsoralen and long wave ultraviolet light.

J. Delhanty, H. Baden, J. Parrington, 1972, Biochimica et biophysica acta.

Specific chromosome aberrations in ataxia telangiectasia.

J. Delhanty, D. Harnden, J. Parrington, 1975, Journal of medical genetics.

Detection of aneuploidy and chromosomal mosaicism in human embryos during preimplantation sex determination by fluorescent in situ hybridisation, (FISH).

D. Griffin, J. Harper, J. Delhanty, 1993, Human molecular genetics.

Unscheduled DNA synthesis, u.v.‐induced chromosome aberrations adn SV40 transformation in cultured cells from xeroderma pigmentosum

J. Delhanty, H. Baden, J. Parrington, 1971, Annals of human genetics.

46 XX KARYOTYPE IN FOUR TISSUES OF A TRUE HERMAPHRODITE

J. Delhanty, M. Lucas, R. M. Haines, 1971, The Journal of obstetrics and gynaecology of the British Commonwealth.

Isolation of fetal cells from transcervical samples by micromanipulation: Molecular confirmation of their fetal origin and diagnosis of fetal aneuploidy

B. Tutschek, M. Adinolfi, J. Delhanty, 1995, Prenatal diagnosis.

Detection of fetal cells in transcervical samples and prenatal diagnosis of chromosomal abnormalities

B. Tutschek, M. Adinolfi, J. Delhanty, 1995, Prenatal diagnosis.

Leucocyte Alkaline Phosphatase in Klinefelter's Syndrome

J. Delhanty, U. Mittwoch, W. Weber, 1965, Journal of medical genetics.

Preimplantation genetic diagnosis of chromosome abnormalities: implications from the outcome for couples with chromosomal rearrangements

C. Rodeck, J. Harper, A. Doshi, 2003, Prenatal diagnosis.

Infertile couples with Robertsonian translocations: preimplantation genetic analysis of embryos reveals chaotic cleavage divisions

J. Harper, J. Delhanty, R. Winston, 1998, Human Genetics.

Mechanisms of aneuploidy induction in human oogenesis and early embryogenesis

J. Delhanty, 2005, Cytogenetic and Genome Research.

The origin of genetic defects in the human and their detection in the preimplantation embryo.

J. Delhanty, A. Handyside, 1995, Human reproduction update.

Mechanisms of maternal aneuploidy: FISH analysis of oocytes and polar bodies in patients undergoing assisted conception

J. Mills, R. Mahmood, J. Delhanty, 2000, Human Genetics.

Chromosome instability in lymphocytes, fibroblasts, and colon epithelial-like cells from patients with familial polyposis coli.

M. Davis, J. Delhanty, J. Wood, 1983, Cancer genetics and cytogenetics.

Cytogenetic and Y chromosome microdeletion screening of a random group of infertile males.

P. Serhal, J. Delhanty, M. Sütterlin, 2003, Fertility and sterility.

Preimplantation Genetic Diagnosis of Inherited Cancer: Familial Adenomatous Polyposis Coli

A. Ao, D. Wells, J. Delhanty, 1998, Journal of Assisted Reproduction and Genetics.

Chromosome Abnormalities in the Human Oocyte

D. Wells, J. Delhanty, E. Fragouli, 2011, Cytogenetic and Genome Research.

Telomere length in human blastocysts.

G. Baio, P. Serhal, J. Delhanty, 2014, Reproductive biomedicine online.

Transcriptomic profiling of human oocytes: association of meiotic aneuploidy and altered oocyte gene expression.

P. Patrizio, J. Delhanty, D. Wells, 2010, Molecular human reproduction.

Aneuploidy screening in direct chorionic villus samples by fluorescence in situ hybridisation: the use of commercial probes in a clinical setting

J. Delhanty, R. Hastings, C. Quilter, 2001, BJOG : an international journal of obstetrics and gynaecology.

Dual fluorescent in situ hybridisation for simultaneous detection of X and Y chromosome-specific probes for the sexing of human preimplantation embryonic nuclei

D. Griffin, L. Wilton, J. Delhanty, 1992, Human Genetics.

The origin and significance of additional aneuploidy events in couples undergoing preimplantation genetic diagnosis for translocations by array comparative genomic hybridization.

P. Serhal, J. Delhanty, S. SenGupta, 2016, Reproductive biomedicine online.

The origin and significance of additional aneuploidy events in couples undergoing PGD for translocations by aCGH

P. Serhal, J. Delhanty, S. SenGupta, 2015 .

Errors in Chromosome Segregation During Oogenesis and Early Embryogenesis

J. Delhanty, M. Hultén, Edward M. Smith, 2010 .

Male and female meiotic behaviour of an intrachromosomal insertion determined by preimplantation genetic diagnosis

A. Doshi, J. Delhanty, D. M. Ranieri, 2010, Molecular Cytogenetics.

Growth of Differentiating Testes and Ovaries

J. Delhanty, F. Beck, U. Mittwoch, 1969, Nature.

Orphan receptors.

J. Dooley, N. Habib, J. Delhanty, 1993, British Journal of Cancer.

Polymorphisms in the MTHFR gene influence embryo viability and the incidence of aneuploidy

S. Bristow, D. Wells, J. Delhanty, 2016, Human Genetics.

The why, the how and the when of PGS 2.0: current practices and expert opinions of fertility specialists, molecular biologists, and embryologists.

J. Vermeesch, M. Meseguer, C. Simón, 2016, Molecular human reproduction.

Mutations truncating the EP300 acetylase in human cancers

Carlos Caldas, Bruce A.J. Ponder, Simon A. Gayther, 2000, Nature Genetics.

Genetic alterations in gastric cancers from British patients.

I. Talbot, D. Wells, J. Delhanty, 2001, Cancer genetics and cytogenetics.

Chromosome analysis by FISH in human preimplantation genetics.

J. Delhanty, 1997, Human reproduction.

How common is germinal mosaicism that leads to premeiotic aneuploidy in the female?

J. Delhanty, S. SenGupta, H. Ghevaria, 2019, Journal of Assisted Reproduction and Genetics.

A trisomic germ cell line and precocious chromatid segregation leads to recurrent trisomy 21 conception

J. Harper, J. Delhanty, R. Winston, 1999, Human Genetics.

Polymorphisms in the MTHFR gene influence embryo viability and the incidence of aneuploidy

S. Bristow, D. Wells, J. Delhanty, 2016, Human Genetics.

Mechanisms of aneuploidy induction in human oogenesis and early embryogenesis.

J. Delhanty, J. Delhanty, 2007, Cytogenetic and genome research.

Inherited Aneuploidy: Germline Mosaicism

J. Delhanty, 2011, Cytogenetic and Genome Research.

Origins of Human Aneuploidy

J. Delhanty, 2010, eLS.

Next Generation Sequencing Detects Premeiotic Errors in Human Oocytes

P. Serhal, J. Delhanty, S. SenGupta, 2022, International journal of molecular sciences.

Variations in humanized and defined culture conditions supporting derivation of new human embryonic stem cell lines.

S. Dhanjal, J. Fletcher, I. Wilmut, 2006, Cloning and stem cells.

Gonadal growth in chick embryos.

J. Delhanty, U. Mittwoch, C. Smith, 1971, Nature: New biology.

Preimplantation genetic diagnosis for retinoblastoma predisposition

S. Dhanjal, J. Harper, A. Doshi, 2006, British Journal of Ophthalmology.

, Alpesh retinoblastoma predisposition Preimplantation genetic diagnosis for

S. Dhanjal, J. Harper, P. Serhal, 2007 .

Comment on: S.S. Prime et al. "A review of inherited cancer syndromes and their relevance to oral squamous cell carcinoma" Oral Oncology 2001;37(1), 1-16.

P. Abou-Sleiman, J. Delhanty, A. Patrikidou, 2002, Oral oncology.

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

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

D12S56: a highly polymorphic locus on human chromosome 12q14

J. Delhanty, J. Wolfe, Z. Ulinowski, 1991, Annals of human genetics.

Linkage analysis in adenomatous polyposis coli: the use of four closely linked DNA probes in 20 UK families.

J. Attwood, J. Burn, M. Davis, 1991, Journal of medical genetics.

Chromosome 5 allele loss in familial and sporadic colorectal adenomas.

J. Jass, J. Delhanty, M. Rees, 1989, British Journal of Cancer.

Aneuploidy in the Human Cleavage Stage Embryo

J. Delhanty, Anna Mantzouratou, 2011, Cytogenetic and Genome Research.

Comparative genomic hybridization analysis of human oocytes and polar bodies.

A. Thornhill, J. Harper, D. Wells, 2006, Human reproduction.

The use of irradiation and fusion gene transfer (IFGT) hybrids to isolate DNA clones from human chromosome region 9q33-q34

P. Goodfellow, D. Griffin, J. Wolfe, 1991, Somatic cell and molecular genetics.

DNA markers in risk calculations . retinal pigment epithelium , and congenital hypertrophy of the polyposis coli : use of age of onset , register for familial adenomatous The UK Northern region genetic

J. Burn, F. Lalloo, J. Delhanty, 2004 .

Detection of hemizygosity at the elastin locus by FISH analysis as a diagnostic test in both classical and atypical cases of Williams syndrome.

J. Delhanty, M. Baraitser, I. Borg, 1995, Journal of medical genetics.

Meiotic outcome in two carriers of Y autosome reciprocal translocations: selective elimination of certain segregants

P. Serhal, J. Delhanty, S. SenGupta, 2017, Molecular Cytogenetics.

Adenomatous polyposis coli and a cytogenetic deletion of chromosome 5 resulting from a maternal intrachromosomal insertion.

J. Barber, J. Delhanty, D. Eccles, 1994, Journal of medical genetics.

Localisation of the human blue cone pigment gene to chromosome band 7q31.3-32

D. Hunt, S. Gayther, J. Fitzgibbon, 2004, Human Genetics.

AN UNUSUAL ACROCENTRIC FOUND IN A CASE OF IDIOCY WITH MICROPHTHALMIA

J. Delhanty, A. Shapiro, 2008 .

Cytogenetic analysis of unfertilized oocytes retrieved after treatment with the LHRH analogue, buserelin.

J. Delhanty, R. Penketh, 1990, Human reproduction.

O-94: Comprehensive characterization of gene expression in human oocytes and identification of perturbations associated with meiotic aneuploidy, maturation and infertile pathology

P. Patrizio, D. Wells, J. Delhanty, 2006 .

The putative tumor suppressor gene on chromosome 5q for hepatocellular carcinoma is distinct from the MCC and APC genes.

J. Dooley, N. Habib, J. Delhanty, 1993, Cancer detection and prevention.

PGD protocols using multiplex fluorescent PCR.

J. Harper, D. Wells, W. Piyamongkol, 2001, Reproductive biomedicine online.

Dde I RFLP may falsify linkage analysis of hereditary retinoblastoma when using SSCP of p88PR0.6 region.

J. Delhanty, M. Sütterlin, P. Sleiman, 2000, Anticancer research.

Genetic instability in patients with metachronous colorectal cancers

J. Delhanty, S. SenGupta, P. Boulos, 1997, The British journal of surgery.

Localization of the gene encoding human phosphatidylinositol transfer protein (PITPN) to 17p13.3: a gene showing homology to the Drosophila retinal degeneration B gene (rdgB).

K. Dulai, D. Hunt, S. Gayther, 1994, Cytogenetics and cell genetics.

Infrequent alterations of the APC and MCC genes in gastric cancers from British patients.

I. Talbot, J. Delhanty, R. Sud, 1996, British Journal of Cancer.

Preimplantation genetic diagnosis

J. Harper, J. Delhanty, 2000, Clinical obstetrics and gynecology.

Preimplantation genetic diagnosis for couples at high risk of Down syndrome pregnancy owing to parental translocation or mosaicism

J. Harper, J. Delhanty, R. Winston, 1999, Journal of medical genetics.

A Mosaic Mongol with Normal Leucocyte Chromosomes

J. Delhanty, M. Ridler, A. Shapiro, 1965, British Journal of Psychiatry.

Infrequent chromosome allele loss in fibrolamellar carcinoma.

J. Dooley, N. Habib, J. Delhanty, 1993, British Journal of Cancer.

TheUK Northern Region genetic register forfamilial adenomatous polyposis coli: useofageofonset, congenital hypertrophy oftheretinal pigment epithelium, andDNA markers inrisk calculations

F. Lalloo, J. Delhanty, W. Church, 2011 .

Comprar Preimplantation Genetic Diagnosis 2Ed | Alan H. Handyside | 9780521884716 | Cambridge University Press

J. Harper, J. Delhanty, A. Handyside, 2009 .

The Development of PGD

Joy D. A. Delhanty, J. Delhanty, 2015 .

The origins of genetic variation between individual human oocytes and embryos: implications for infertility

J. Delhanty, 2013, Human fertility.

Genetic instability in patients with metachronous colorectal cancers

J. Delhanty, S. SenGupta, P. Boulos, 1997, The British journal of surgery.

Modification of the triplet repeat primed polymerase chain reaction method for detection of the CTG repeat expansion in myotonic dystrophy type 1: application in preimplantation genetic diagnosis.

S. Dhanjal, P. Serhal, J. Delhanty, 2010, Fertility and sterility.

An atlas of preimplantation genetic diagnosis

J. Delhanty, 2001 .

Lack of demonstrable chromosome allele loss in hepatocellular adenoma.

J. Dooley, N. Habib, J. Delhanty, 1993, International journal of oncology.

A Novel Methodology Allows Detection of Every Chromosome in Single Blastomeres from Human Preimplantation Embryos and Reveals Aneuploidy, Mosaicism and Uniformly Normal Embryos

D. Wells, J. Delhanty, 2000 .

Increased chromosome breakage by N-methyl-N1-nitro-N-nitrosoguanidine in patients with adenomatous polyposis coli.

J. Delhanty, J. Delhanty, H. Cooke, 1989, Cancer genetics and cytogenetics.

Modification of the triplet repeat primed polymerase chain reaction method for detection of the CTG repeat expansion in myotonic dystrophy type 1: application in preimplantation genetic diagnosis.

S. Dhanjal, P. Serhal, J. Delhanty, 2010, Fertility and sterility.

The UK Northern region genetic register for familial adenomatous polyposis coli: use of age of onset, congenital hypertrophy of the retinal pigment epithelium, and DNA markers in risk calculations.

F. Lalloo, J. Delhanty, M. Cachón-González, 1991, Journal of medical genetics.

Isolation of new therapeutically suitable human embryo stem cell lines without direct exposure to animal cell products

S. Dhanjal, J. Fletcher, I. Wilmut, 2006 .

Rapid detection of rare variants and common polymorphisms in the APC gene by PCR-SSCP for presymptomatic diagnosis and showing allele loss.

S. Gayther, D. Wells, J. Delhanty, 1995, Journal of medical genetics.

The why, the how and the when of PGS 2.0: current practices and expert opinions of fertility specialists, molecular biologists, and embryologists.

J. Vermeesch, M. Meseguer, C. Simón, 2016, Molecular human reproduction.

Is the polar body approach best for pre-implantation genetic screening?

J. Delhanty, 2011, Placenta.