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J D A Delhanty

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Co-Publications
Name
28
Harper, Joyce
16
Winston, Robert
15
Wells, Dagan
14
Handyside, AH
13
Serhal, Paul
8
Fragouli, Elpida
7
Doshi, Alpesh
7
Habib, Nagy
6
Abou-Sleiman, Patrick
6
Sherlock, Jon
5
Parrington, John
4
Quilter, Claire
4
Rodeck, Charles
4
Conn, CM
4
Apessos, Angela

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Publications

TOP 3
Daphnis D D; Fragouli E; Economou K; Jerkovic S; Craft I L; Delhanty J D A; Harper J C
Analysis of the evolution of chromosome abnormalities in human embryos from Day 3 to 5 using CGH and FISH.
Dhanjal Seema; Kakourou Georgia; Mamas Thalia; Saleh Natasha; Doshi Alpesh; Gotts Sarah; Nuttall Sarah; Fordham Karen; Serhal Paul; Delhanty Joy; Harper Joyce; Sengupta Sioban
Preimplantation genetic diagnosis for retinoblastoma predisposition.
Fragouli Elpida; Delhanty Joy D A; Wells Dagan
Single cell diagnosis using comparative genomic hybridization after preliminary DNA amplification still needs more tweaking: too many miscalls.

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All Publications

2008: Daphnis D D; Fragouli E; Economou K; Jerkovic S; Craft I L; Delhanty J D A; Harper J C
Analysis of the evolution of chromosome abnormalities in human embryos from Day 3 to 5 using CGH and FISH.
Molecular human reproduction 2008;14(2):117-25.
2007: Dhanjal Seema; Kakourou Georgia; Mamas Thalia; Saleh Natasha; Doshi Alpesh; Gotts Sarah; Nuttall Sarah; Fordham Karen; Serhal Paul; Delhanty Joy; Harper Joyce; Sengupta Sioban
Preimplantation genetic diagnosis for retinoblastoma predisposition.
The British journal of ophthalmology 2007;91(8):1090-1.
2007: Fragouli Elpida; Delhanty Joy D A; Wells Dagan
Single cell diagnosis using comparative genomic hybridization after preliminary DNA amplification still needs more tweaking: too many miscalls.
Fertility and sterility 2007;88(1):247-8; author reply 248-9.
2007: Mantzouratou A; Mania A; Fragouli E; Xanthopoulou L; Tashkandi S; Fordham K; Ranieri D M; Doshi A; Nuttall S; Harper J C; Serhal P; Delhanty J D A
Variable aneuploidy mechanisms in embryos from couples with poor reproductive histories undergoing preimplantation genetic screening.
Human reproduction (Oxford, England) 2007;22(7):1844-53.
2007: Kakourou Georgia; Dhanjal Seema; Daphnis Danny; Doshi Alpesh; Nuttall Sarah; Gotts Sarah; Serhal Paul; Delhanty Joy; Harper Joyce; SenGupta Sioban
Preimplantation genetic diagnosis for myotonic dystrophy type 1: detection of crossover between the gene and the linked marker APOC2.
Prenatal diagnosis 2007;27(2):111-6.
2006: Fragouli E; Wells D; Thornhill A; Serhal P; Faed M J W; Harper J C; Delhanty J D A
Comparative genomic hybridization analysis of human oocytes and polar bodies.
Human reproduction (Oxford, England) 2006;21(9):2319-28.
2006: Fragouli Elpida; Wells Dagan; Doshi Alpesh; Gotts Sarah; Harper Joyce C; Delhanty Joy D A
Complete cytogenetic investigation of oocytes from a young cancer patient with the use of comparative genomic hybridisation reveals meiotic errors.
Prenatal diagnosis 2006;26(1):71-6.
2006: Fletcher Judy M; Ferrier Patricia M; Gardner John O; Harkness Linda; Dhanjal Seema; Serhal Paul; Harper Joyce; Delhanty Joy; Brownstein David G; Prasad Yogesh R; Lebkowski Jane; Mandalam Ram; Wilmut Ian; De Sousa Paul A
Variations in humanized and defined culture conditions supporting derivation of new human embryonic stem cell lines.
Cloning and stem cells 2006;8(4):319-34.
2006: Fragouli E; Wells D; Whalley K M; Mills J A; Faed M J W; Delhanty J D A
Increased susceptibility to maternal aneuploidy demonstrated by comparative genomic hybridization analysis of human MII oocytes and first polar bodies.
Cytogenetic and genome research 2006;114(1):30-8.
2005: Wells D; Bermudez M G; Steuerwald N; Thornhill A R; Walker D L; Malter H; Delhanty J D A; Cohen J
Expression of genes regulating chromosome segregation, the cell cycle and apoptosis during human preimplantation development.
Human reproduction (Oxford, England) 2005;20(5):1339-48.
2005: Daphnis D D; Delhanty J D A; Jerkovic S; Geyer J; Craft I; Harper J C
Detailed FISH analysis of day 5 human embryos reveals the mechanisms leading to mosaic aneuploidy.
Human reproduction (Oxford, England) 2005;20(1):129-37.
2005: Delhanty J D A
Mechanisms of aneuploidy induction in human oogenesis and early embryogenesis.
Cytogenetic and genome research 2005;111(3-4):237-44.
2004: Delhanty Joy D A
PGD for reciprocal translocations.
Prenatal diagnosis 2004;24(7):552.
2004: Harper Joyce C; Pergament Eugene; Delhanty Joy D A
Genetics of gametes and embryos.
European journal of obstetrics, gynecology, and reproductive biology 2004;115 Suppl 1():S80-4.
2003: Cupisti S; Conn C M; Fragouli E; Whalley K; Mills J A; Faed M J W; Delhanty J D A
Sequential FISH analysis of oocytes and polar bodies reveals aneuploidy mechanisms.
Prenatal diagnosis 2003;23(8):663-8.
2003: Simopoulou M; Harper J C; Fragouli E; Mantzouratou A; Speyer B E; Serhal P; Ranieri D M; Doshi A; Henderson J; Rodeck C H; Delhanty J D A
Preimplantation genetic diagnosis of chromosome abnormalities: implications from the outcome for couples with chromosomal rearrangements.
Prenatal diagnosis 2003;23(8):652-62.
2003: Delhanty J D A
Beta thalassaemia: fetal HLA typing.
Lancet 2003;362(9377):6.
2003: Quilter Claire R; Svennevik Elizabeth C; Serhal Paul; Ralph David; Bahadur Gulam; Stanhope Richard; Sütterlin Marc; Delhanty Joy D A; Taylor Kay E
Cytogenetic and Y chromosome microdeletion screening of a random group of infertile males.
Fertility and sterility 2003;79(2):301-7.
2002: Quilter C R; Nathwani N; Conway G S; Stanhope R; Ralph D; Bahadur G; Serhal P; Taylor K; Delhanty J D A
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.
Journal of medical genetics 2002;39(12):e80.
2002: Delhanty Joy D A; Wells Dagan
Preimplantation genetic diagnosis: an alternative to prenatal diagnosis.
Expert review of molecular diagnostics 2002;2(5):395-9.
2002: Wells Dagan; Escudero Tomas; Levy Brynn; Hirschhorn Kurt; Delhanty Joy D A; Munné Santiago
First clinical application of comparative genomic hybridization and polar body testing for preimplantation genetic diagnosis of aneuploidy.
Fertility and sterility 2002;78(3):543-9.
2002: Harper Joyce C; Wells Dagan; Piyamongkol Wirawit; Abou-Sleiman Patrick; Apessos Angela; Ioulianos Antonis; Davis Mary; Doshi Alpesh; Serhal Paul; Ranieri Massimo; Rodeck Charles; Delhanty Joy D A
Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disorders.
Prenatal diagnosis 2002;22(6):525-33.
2002: Abou-Sleiman P M; Apessos A; Harper J C; Serhal P; Winston R M L; Delhanty J D A
First application of preimplantation genetic diagnosis to neurofibromatosis type 2 (NF2).
Prenatal diagnosis 2002;22(6):519-24.
2002: Patrikidou Anna; Bennett Jon; Abou-Sleiman Patrick; Delhanty Joy D A; Harris Malcolm
A novel, de novo germline TP53 mutation in a rare presentation of the Li-Fraumeni syndrome in the maxilla.
Oral oncology 2002;38(4):383-90.
2002: Abou-Sleiman P M; Apessos A; Harper J C; Serhal P; Delhanty J D A
Pregnancy following preimplantation genetic diagnosis for Crouzon syndrome.
Molecular human reproduction 2002;8(3):304-9.
2002: Patrikidou Anna; Harris Malcolm; Bennett Jon; Abou-Sleiman Patrick; Delhanty Joy D A
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.
Oral oncology 2002;38(2):216-7.
2001: Piyamongkol W; Harper J C; Delhanty J D; Wells D
Preimplantation genetic diagnostic protocols for alpha- and beta-thalassaemias using multiplex fluorescent PCR.
Prenatal diagnosis 2001;21(9):753-9.
2001: Delhanty J D
Preimplantation genetics: an explanation for poor human fertility?
Annals of human genetics 2001;65(Pt 4):331-8.
2001: Apessos A; Abou-Sleiman P M; Harper J C; Delhanty J D
Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers.
Prenatal diagnosis 2001;21(6):504-11.
2001: Piyamongkol W; Harper J C; Sherlock J K; Doshi A; Serhal P F; Delhanty J D; Wells D
A successful strategy for preimplantation genetic diagnosis of myotonic dystrophy using multiplex fluorescent PCR.
Prenatal diagnosis 2001;21(3):223-32.
2001: Quilter C R; Holman S; AL-Hammadi R M; Theodorides D; Hastings R J; Delhanty J D
Aneuploidy screening in direct chorionic villus samples by fluorescence in situ hybridisation: the use of commercial probes in a clinical setting.
BJOG : an international journal of obstetrics and gynaecology 2001;108(2):215-8.
2001: Wells D; Delhanty J D
Preimplantation genetic diagnosis: applications for molecular medicine.
Trends in molecular medicine 2001;7(1):23-30.
2000: Sütterlin M W; Sleiman P A; Price E; Onadim Z; Delhanty J
Dde I RFLP may falsify linkage analysis of hereditary retinoblastoma when using SSCP of p88PR0.6 region.
Anticancer research 2000;20(6D):5233-6.
2000: Wells D; Delhanty J D
Comprehensive chromosomal analysis of human preimplantation embryos using whole genome amplification and single cell comparative genomic hybridization.
Molecular human reproduction 2000;6(11):1055-62.
2000: Delhanty J D; Harper J C
Pre-implantation genetic diagnosis.
Baillière's best practice & research. Clinical obstetrics & gynaecology 2000;14(4):691-708.
2000: Ioulianos A; Wells D; Harper J C; Delhanty J D
A successful strategy for preimplantation diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.
Prenatal diagnosis 2000;20(7):593-8.
2000: Ruangvutilert P; Delhanty J D; Serhal P; Simopoulou M; Rodeck C H; Harper J C
FISH analysis on day 5 post-insemination of human arrested and blastocyst stage embryos.
Prenatal diagnosis 2000;20(7):552-60.
2000: Mahmood R; Brierley C H; Faed M J; Mills J A; Delhanty J D
Mechanisms of maternal aneuploidy: FISH analysis of oocytes and polar bodies in patients undergoing assisted conception.
Human genetics 2000;106(6):620-6.
2000: Harper J C; Delhanty J D
Preimplantation genetic diagnosis.
Current opinion in obstetrics & gynecology 2000;12(2):67-72.
2000: Hastings R J; Svennevik E C; Setterfield B; Wells D; Delhanty J D; Mackinnon H
Deletion and duplication of the adenomatous polyposis coli gene resulting from an interchromosomal insertion involving 5(q22q23.3) in the father.
Journal of medical genetics 2000;37(2):141-5.
2000: Ruangvutilert P; Delhanty J D; Rodeck C H; Harper J C
Relative efficiency of FISH on metaphase and interphase nuclei from non-mosaic trisomic or triploid fibroblast cultures.
Prenatal diagnosis 2000;20(2):159-62.
1999: Sütterlin M; Sleiman P A; Onadim Z; Delhanty J
Single cell detection of inherited retinoblastoma predisposition.
Prenatal diagnosis 1999;19(13):1231-6.
1999: Wells D; Sherlock J K; Handyside A H; Delhanty J D
Detailed chromosomal and molecular genetic analysis of single cells by whole genome amplification and comparative genomic hybridisation.
Nucleic acids research 1999;27(4):1214-8.
1999: Cozzi J; Conn C M; Harper J; Winston R M; Rindl M; Farndon P A; Delhanty J D
A trisomic germ cell line and precocious chromatid segregation leads to recurrent trisomy 21 conception.
Human genetics 1999;104(1):23-8.
1999: Conn C M; Cozzi J; Harper J C; Winston R M; Delhanty J D
Preimplantation genetic diagnosis for couples at high risk of Down syndrome pregnancy owing to parental translocation or mosaicism.
Journal of medical genetics 1999;36(1):45-50.
1998: Harper J; Pergament E; Delhanty J
Recent advances in molecular and molecular cytogenetic techniques have enabled the diagnosis of some inherited diseases from a single cell.
Prenatal diagnosis 1998;18(13):1343-4.
1998: Quilter C R; Taylor K; Conway G S; Nathwani N; Delhanty J D
Cytogenetic and molecular investigations of Y chromosome sequences and their role in Turner syndrome.
Annals of human genetics 1998;62(Pt 2):99-106.
1998: Ao A; Wells D; Handyside A H; Winston R M; Delhanty J D
Preimplantation genetic diagnosis of inherited cancer: familial adenomatous polyposis coli.
Journal of assisted reproduction and genetics 1998;15(3):140-4.
1998: Conn C M; Harper J C; Winston R M; Delhanty J D
Infertile couples with Robertsonian translocations: preimplantation genetic analysis of embryos reveals chaotic cleavage divisions.
Human genetics 1998;102(1):117-23.
1997: Delhanty J D
Chromosome analysis by FISH in human preimplantation genetics.
Human reproduction (Oxford, England) 1997;12(11 Suppl):153-5.
1997: El-Hashemite N; Delhanty J D
A technique for eliminating allele specific amplification failure during DNA amplification of heterozygous cells for preimplantation diagnosis.
Molecular human reproduction 1997;3(11):975-8.
1997: Delhanty J D; Wells D; Harper J C
Genetic diagnosis before implantation.
BMJ (Clinical research ed.) 1997;315(7112):828-9.
1997: el-Hashemite N; Wells D; Delhanty J D
Single cell detection of beta-thalassaemia mutations using silver stained SSCP analysis: an application for preimplantation diagnosis.
Molecular human reproduction 1997;3(8):693-8.
1997: Handyside A H; Delhanty J D
Preimplantation genetic diagnosis: strategies and surprises.
Trends in genetics : TIG 1997;13(7):270-5.
1997: Delhanty J D; Harper J C; Ao A; Handyside A H; Winston R M
Multicolour FISH detects frequent chromosomal mosaicism and chaotic division in normal preimplantation embryos from fertile patients.
Human genetics 1997;99(6):755-60.
1997: Sherlock J; Halder A; Tutschek B; Delhanty J; Rodeck C; Adinolfi M
Prenatal detection of fetal aneuploidies using transcervical cell samples.
Journal of medical genetics 1997;34(4):302-5.
1997: el-Hashemite N; Petrou M; Khalifa A S; Heshmat N M; Rady M S; Delhanty J D
Identification of novel Asian Indian and Japanese mutations causing beta-thalassaemia in the Egyptian population.
Human genetics 1997;99(2):271-4.
1996: Sud R; Talbot I C; Delhanty J D
Infrequent alterations of the APC and MCC genes in gastric cancers from British patients.
British journal of cancer 1996;74(7):1104-8.
1996: el-Hashemite N; Wells D; Delhanty J D
Preimplantation genetic diagnosis of beta-thalassaemia.
Lancet 1996;348(9027):620-1.
1996: Fitzgibbon J; Katsanis N; Wells D; Delhanty J; Vallins W; Hunt D M
Human guanylate kinase (GUK1): cDNA sequence, expression and chromosomal localisation.
FEBS letters 1996;385(3):185-8.
1996: Sherlock J K; Griffin D K; Delhanty J D; Parrington J M
Homologies between human and marmoset (Callithrix jacchus) chromosomes revealed by comparative chromosome painting.
Genomics 1996;33(2):214-9.
1996: Harper J C; Delhanty J D
Detection of chromosomal abnormalities in human preimplantation embryos using FISH.
Journal of assisted reproduction and genetics 1996;13(2):137-9.
1996: Wells D; Chapman P; Landgrebe J C; Tsioupra K; Delhanty J D
Four novel germline mutations of the APC gene.
Human mutation 1996;8(2):193-5.
1995: Harper J C; Dawson K; Delhanty J D; Winston R M
The use of fluorescent in-situ hybridization (FISH) for the analysis of in-vitro fertilization embryos: a diagnostic tool for the infertile couple.
Human reproduction (Oxford, England) 1995;10(12):3255-8.
1995: Fitzgibbon J; Wells D; Pilz A; Delhanty J; Kai M; Kanoh H; Hunt D
Localisation of the gene encoding diacylglycerol kinase 3 (DAGK3) to human chromosome 3q27-28 and mouse chromosome 16.
Current eye research 1995;14(11):1041-3.
1995: Tutschek B; Sherlock J; Halder A; Delhanty J; Rodeck C; Adinolfi M
Isolation of fetal cells from transcervical samples by micromanipulation: molecular confirmation of their fetal origin and diagnosis of fetal aneuploidy.
Prenatal diagnosis 1995;15(10):951-60.
1995: Adinolfi M; Sherlock J; Tutschek B; Halder A; Delhanty J; Rodeck C
Detection of fetal cells in transcervical samples and prenatal diagnosis of chromosomal abnormalities.
Prenatal diagnosis 1995;15(10):943-9.
1995: al-Jehani R M; Povey S; Delhanty J D; Parrington J M
Loss of heterozygosity on chromosome arms 5q, 11p, 11q, 13q, and 16p in human testicular germ cell tumors.
Genes, chromosomes & cancer 1995;13(4):249-56.
1995: Gayther S A; Sud R; Wells D; Tsioupra K; Delhanty J D
Rapid detection of rare variants and common polymorphisms in the APC gene by PCR-SSCP for presymptomatic diagnosis and showing allele loss.
Journal of medical genetics 1995;32(7):568-71.
1995: Delhanty J D; Handyside A H
The origin of genetic defects in the human and their detection in the preimplantation embryo.
Human reproduction update 1995;1(3):201-15.
1995: Delhanty J D; Tsioupra K
Haplotype comparison in fresh mutation cases of adenomatous polyposis coli due to deletion AAAGA at codon 1309.
Annals of human genetics 1995;59(Pt 1):39-42.
1995: Harper J C; Coonen E; Handyside A H; Winston R M; Hopman A H; Delhanty J D
Mosaicism of autosomes and sex chromosomes in morphologically normal, monospermic preimplantation human embryos.
Prenatal diagnosis 1995;15(1):41-9.
1994: Coonen E; Harper J C; Ramaekers F C; Delhanty J D; Hopman A H; Geraedts J P; Handyside A H
Presence of chromosomal mosaicism in abnormal preimplantation embryos detected by fluorescence in situ hybridisation.
Human genetics 1994;94(6):609-15.
1994: Delhanty J D
Preimplantation diagnosis.
Prenatal diagnosis 1994;14(13):1217-27.
1994: Harper J C; Robinson F; Duffy S; Griffin D K; Handyside A H; Delhanty J D; Winston R M
Detection of fertilization in embryos with accelerated cleavage by fluorescent in-situ hybridization (FISH).
Human reproduction (Oxford, England) 1994;9(9):1733-7.
1994: Ding S F; Delhanty J D; Zografos G; Michail N E; Dooley J S; Habib N A
Chromosome allele loss in colorectal liver metastases and its association with clinical features.
The British journal of surgery 1994;81(6):875-8.
1994: Gayther S A; Rees M; Delhanty J D
Frequent normal allele loss and maternal origin of the mutation shown by DNA homoduplex analysis in a severely affected patient with adenomatous polyposis coli.
Annals of human genetics 1994;58(Pt 2):101-6.
1994: Harper J C; Coonen E; Ramaekers F C; Delhanty J D; Handyside A H; Winston R M; Hopman A H
Identification of the sex of human preimplantation embryos in two hours using an improved spreading method and fluorescent in-situ hybridization (FISH) using directly labelled probes.
Human reproduction (Oxford, England) 1994;9(4):721-4.
1994: Fitzgibbon J; Appukuttan B; Gayther S; Wells D; Delhanty J; Hunt D M
Localisation of the human blue cone pigment gene to chromosome band 7q31.3-32.
Human genetics 1994;93(1):79-80.
1994: Gayther S A; Wells D; SenGupta S B; Chapman P; Neale K; Tsioupra K; Delhanty J D
Regionally clustered APC mutations are associated with a severe phenotype and occur at a high frequency in new mutation cases of adenomatous polyposis coli.
Human molecular genetics 1994;3(1):53-6.
1994: Fitzgibbon J; Pilz A; Gayther S; Appukuttan B; Dulai K S; Delhanty J D; Helmkamp G M; Yarbrough L R; Hunt D M
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).
Cytogenetics and cell genetics 1994;67(3):205-7.
1993: Delhanty J D; Griffin D K; Handyside A H; Harper J; Atkinson G H; Pieters M H; Winston R M
Detection of aneuploidy and chromosomal mosaicism in human embryos during preimplantation sex determination by fluorescent in situ hybridisation, (FISH).
Human molecular genetics 1993;2(8):1183-5.
1993: Gayther S; Wells D; Gulati K; Chapman P; Burn J; Delhanty J D
Germline rearrangement of MCC and APC detected by pulsed field gel electrophoresis and fluorescent in situ hybridization.
Annals of human genetics 1993;57(Pt 3):169-78.
1993: Griffin D K; Wilton L J; Handyside A H; Atkinson G H; Winston R M; Delhanty J D
Diagnosis of sex in preimplantation embryos by fluorescent in situ hybridisation.
BMJ (Clinical research ed.) 1993;306(6889):1382.
1993: Rees M; Leigh S E; Delhanty J D; Bowles L; Talbot I C
Molecular genetic evidence for the delineation of a more severe form of familial adenomatous polyposis which results from fresh mutation.
Annals of human genetics 1993;57(Pt 2):97-104.
1993: Ding S F; Delhanty J D; Bowles L; Dooley J S; Wood C B; Habib N A
Loss of constitutional heterozygosity on chromosomes 5 and 17 in cholangiocarcinoma.
British journal of cancer 1993;67(5):1007-10.
1993: Ding S F; Delhanty J D; Bowles L; Dooley J S; Wood C B; Habib N A
Infrequent chromosome allele loss in fibrolamellar carcinoma.
British journal of cancer 1993;67(2):244-6.
1993: Ding S F; Delhanty J D; Dooley J S; Bowles L; Wood C B; Habib N A
The putative tumor suppressor gene on chromosome 5q for hepatocellular carcinoma is distinct from the MCC and APC genes.
Cancer detection and prevention 1993;17(3):405-9.
1992: Ding S F; Jalleh R P; Wood C B; Bowles L; Delhanty J D; Dooley J; Habib N A
Different DNA changes in primary and recurrent hepatocellular carcinoma.
Gut 1992;33(10):1433-5.
1992: Ding S F; Habib N A; Delhanty J D; Bowles L; Greco L; Wood C; Williamson R C; Dooley J S
Loss of heterozygosity on chromosomes 1 and 11 in carcinoma of the pancreas.
British journal of cancer 1992;65(6):809-12.
1992: Griffin D K; Wilton L J; Handyside A H; Winston R M; Delhanty J D
Dual fluorescent in situ hybridisation for simultaneous detection of X and Y chromosome-specific probes for the sexing of human preimplantation embryonic nuclei.
Human genetics 1992;89(1):18-22.
1992: Cross I; Delhanty J; Chapman P; Bowles L V; Griffin D; Wolstenholme J; Bradburn M; Brown J; Wood C; Gunn A
An intrachromosomal insertion causing 5q22 deletion and familial adenomatous polyposis coli in two generations.
Journal of medical genetics 1992;29(3):175-9.
1992: Cachon Gonzalez M B; Wolfe J; Delhanty J D
Dinucleotide repeat polymorphism at the D5S98 locus.
Nucleic acids research 1992;20(4):924.
1991: Ding S F; Habib N A; Dooley J; Wood C; Bowles L; Delhanty J D
Loss of constitutional heterozygosity on chromosome 5q in hepatocellular carcinoma without cirrhosis.
British journal of cancer 1991;64(6):1083-7.
1991: Ulinowski Z; Taylor K; Griffin D; Delhanty J; Wolfe J
D12S56: a highly polymorphic locus on human chromosome 12q14.
Annals of human genetics 1991;55(Pt 4):279-82.
1991: Cachon-Gonzalez M B; Delhanty J D; Burn J; Tsioupra K; Davis M B; Attwood J; Chapman P
Linkage analysis in adenomatous polyposis coli: the use of four closely linked DNA probes in 20 UK families.
Journal of medical genetics 1991;28(10):681-5.
1991: Florian F; Hornigold N; Griffin D K; Delhanty J D; Sefton L; Abbott C; Jones C; Goodfellow P N; Wolfe J
The use of irradiation and fusion gene transfer (IFGT) hybrids to isolate DNA clones from human chromosome region 9q33-q34.
Somatic cell and molecular genetics 1991;17(5):445-53.
1991: Burn J; Chapman P; Delhanty J; Wood C; Lalloo F; Cachon-Gonzalez M B; Tsioupra K; Church W; Rhodes M; Gunn A
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.
Journal of medical genetics 1991;28(5):289-96.
1991: Griffin D K; Handyside A H; Penketh R J; Winston R M; Delhanty J D
Fluorescent in-situ hybridization to interphase nuclei of human preimplantation embryos with X and Y chromosome specific probes.
Human reproduction (Oxford, England) 1991;6(1):101-5.
1990: Bunker C B; Atherton D; Gray O P; Tsioupra K; Delhanty J D; Dowd P M
Familial Raynaud's phenomenon and localized scleroderma associated with essential telangiectasia and cytogenetic abnormalities.
Journal of the Royal Society of Medicine 1990;83(8):531-2.
1990: Delhanty J D; Penketh R J
Cytogenetic analysis of unfertilized oocytes retrieved after treatment with the LHRH analogue, buserelin.
Human reproduction (Oxford, England) 1990;5(6):699-702.
1990: Khouzam M N; Tsioupra K; Delhanty J D
Chromosome breakage in lymphocytes from members of cancer families showing autosomal dominant inheritance.
Clinical genetics 1990;38(1):51-6.
1990: Griffin D K; Leigh S E; Delhanty J D
Use of fluorescent in situ hybridisation to confirm trisomy of chromosome region 1q32-qter as the sole karyotypic defect in a colon cancer cell line.
Genes, chromosomes & cancer 1990;1(4):281-3.
1989: Delhanty J D; Cooke H M
Increased chromosome breakage by N-methyl-N1-nitro-N-nitrosoguanidine in patients with adenomatous polyposis coli.
Cancer genetics and cytogenetics 1989;42(2):263-71.
1989: Delhanty J D
Rapid chromosomal sexing of birds by direct and short term culture techniques.
The Veterinary record 1989;125(4):92.
1989: Penketh R J; Delhanty J D; van den Berghe J A; Finklestone E M; Handyside A H; Malcolm S; Winston R M
Rapid sexing of human embryos by non-radioactive in situ hybridization: potential for preimplantation diagnosis of X-linked disorders.
Prenatal diagnosis 1989;9(7):489-99.
1989: Rees M; Leigh S E; Delhanty J D; Jass J R
Chromosome 5 allele loss in familial and sporadic colorectal adenomas.
British journal of cancer 1989;59(3):361-5.
1989: Handyside A H; Pattinson J K; Penketh R J; Delhanty J D; Winston R M; Tuddenham E G
Biopsy of human preimplantation embryos and sexing by DNA amplification.
Lancet 1989;1(8634):347-9.
1988: Delhanty J D; Parrington J M
The origin of isochromosomes.
Clinical genetics 1988;34(3):207-8.
1988: Aldred M A; Rees M; Tsioupra K; Leigh S E; Neale K F; Delhanty J D
Familial polyposis coli.
Lancet 1988;2(8610):565.
1988: Delhanty J D; Rider S H
Transformation studies on human fibroblasts from familial polyposis coli patients and normal donors.
Mutation research 1988;199(2):327-39.
1988: Tsioupra K; West L F; Davis M B; Parrington J M; Delhanty J D
Spontaneous and induced chromosome damage in lymphocytes of medullary thyroid carcinoma patients and their family members.
Disease markers 1988;6(2):127-32.
1988: Mazzullo H A; Attwood J; Delhanty J D
Familial polyposis coli: no evidence for increased sensitivity to mitomycin C.
Journal of medical genetics 1988;25(4):233-7.
1986: Cooke H M; Penketh R J; Delhanty J D
An evaluation of maternal cell contamination in cultures of chorionic villi for the prenatal diagnosis of chromosome abnormalities.
Clinical genetics 1986;30(6):485-93.
1981: Delhanty J D; Parrington J M; Casey G; Attwood J; West L; Kirk D; Corney G
Growth, DNA repair, sister chromatid exchange and chromosome studies in fibroblasts from Huntington's disease patients.
Annals of human genetics 1981;45(Pt 2):181-98.

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