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J D A Delhanty

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L Xanthopoulou; Alpesh Doshi; H Ghevaria; A Mantzouratou; Paul Serhal; J D A Delhanty
Chromosome breakage in human preimplantation embryos from carriers of structural chromosomal abnormalities in relation to fragile sites, maternal age, and poor sperm factors.
L Xanthopoulou; C Ghebo; H Ghevaria; A Mania; A Mantzouratou; Paul Serhal; J D A Delhanty
When is old too old for preimplantation genetic diagnosis for reciprocal translocations?
L Xanthopoulou; J D A Delhanty; A Mania; T Mamas; Paul Serhal; Sioban SenGupta; A Mantzouratou
The nature and origin of binucleate cells in human preimplantation embryos: relevance to placental mesenchymal dysplasia.

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2012: L Xanthopoulou; Alpesh Doshi; H Ghevaria; A Mantzouratou; Paul Serhal; J D A Delhanty
Chromosome breakage in human preimplantation embryos from carriers of structural chromosomal abnormalities in relation to fragile sites, maternal age, and poor sperm factors.
Cytogenetic and genome research 2012;136(1):21-9.
2011: L Xanthopoulou; C Ghebo; H Ghevaria; A Mania; A Mantzouratou; Paul Serhal; J D A Delhanty
When is old too old for preimplantation genetic diagnosis for reciprocal translocations?
Prenatal diagnosis 2011;31(10):1002-6.
2011: L Xanthopoulou; J D A Delhanty; A Mania; T Mamas; Paul Serhal; Sioban SenGupta; A Mantzouratou
The nature and origin of binucleate cells in human preimplantation embryos: relevance to placental mesenchymal dysplasia.
Reproductive biomedicine online 2011;22(4):362-70.
2011: J D A Delhanty
Inherited aneuploidy: germline mosaicism.
Cytogenetic and genome research 2011;133(2-4):136-40.
2011: A Mantzouratou; J D A Delhanty
Aneuploidy in the human cleavage stage embryo.
Cytogenetic and genome research 2011;133(2-4):141-8.
2011: Elpida Fragouli; Dagan Wells; J D A Delhanty
Chromosome abnormalities in the human oocyte.
Cytogenetic and genome research 2011;133(2-4):107-18.
2010: Georgia Kakourou; Seema Dhanjal; Thalia Mamas; Paul Serhal; J D A Delhanty; Sioban B SenGupta
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.
Fertility and sterility 2010;94(5):1674-9.
2010: Elpida Fragouli; Veronica Bianchi; Pasquale Patrizio; A Obradors; Z Huang; Andrea Borini; J D A Delhanty; Dagan Wells
Transcriptomic profiling of human oocytes: association of meiotic aneuploidy and altered oocyte gene expression.
Molecular human reproduction 2010;16(8):570-82.
2010: B E Speyer; Arnold Pizzey; M Ranieri; R Joshi; J D A Delhanty; Paul Serhal
Fall in implantation rates following ICSI with sperm with high DNA fragmentation.
Human reproduction (Oxford, England) 2010;25(7):1609-18.
2008: D D Daphnis; Elpida Fragouli; K Economou; S Jerkovic; I L Craft; J D A Delhanty; Joyce C Harper
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: Seema Dhanjal; Georgia Kakourou; Thalia Mamas; Natasha Saleh; Alpesh Doshi; Sarah Gotts; Sarah Nuttall; Karen Fordham; Paul Serhal; J D A Delhanty; Joyce Harper; Sioban SenGupta
Preimplantation genetic diagnosis for retinoblastoma predisposition.
The British journal of ophthalmology 2007;91(8):1090-1.
2007: Elpida Fragouli; J D A Delhanty; Dagan Wells
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: A Mantzouratou; A Mania; Elpida Fragouli; L Xanthopoulou; S Tashkandi; K Fordham; Domenico Massimo Ranieri; Alpesh Doshi; Sarah Nuttall; Joyce C Harper; Paul Serhal; J D A Delhanty
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: Georgia Kakourou; Seema Dhanjal; Danny Daphnis; Alpesh Doshi; Sarah Nuttall; Sarah Gotts; Paul Serhal; J D A Delhanty; Joyce Harper; Sioban SenGupta
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: Elpida Fragouli; Dagan Wells; Alan R Thornhill; Paul Serhal; M J W Faed; Joyce C Harper; J D A Delhanty
Comparative genomic hybridization analysis of human oocytes and polar bodies.
Human reproduction (Oxford, England) 2006;21(9):2319-28.
2006: Judy M Fletcher; Patricia M Ferrier; John O Gardner; Linda Harkness; Seema Dhanjal; Paul Serhal; Joyce Harper; J D A Delhanty; David G Brownstein; Yogesh R Prasad; Jane Lebkowski; Ramkumar Mandalam; Ian Wilmut; Paul A De Sousa
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: Elpida Fragouli; Dagan Wells; K M Whalley; JA Mills; M J W Faed; J D A Delhanty
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.
2006: Elpida Fragouli; Dagan Wells; Alpesh Doshi; Sarah Gotts; Joyce C Harper; J D A Delhanty
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.
2005: Dagan Wells; M G Bermudez; Nury M Steuerwald; Alan R Thornhill; David L Walker; Henry E Malter; J D A Delhanty; Jacques Cohen
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: J D A Delhanty
Mechanisms of aneuploidy induction in human oogenesis and early embryogenesis.
Cytogenetic and genome research 2005;111(3-4):237-44.
2005: D D Daphnis; J D A Delhanty; S Jerkovic; J Geyer; I Craft; Joyce C Harper
Detailed FISH analysis of day 5 human embryos reveals the mechanisms leading to mosaic aneuploidy.
Human reproduction (Oxford, England) 2005;20(1):129-37.
2004: J D A Delhanty
PGD for reciprocal translocations.
Prenatal diagnosis 2004;24(7):552.
2004: Joyce C Harper; Eugene Pergament; J D A Delhanty
Genetics of gametes and embryos.
European journal of obstetrics, gynecology, and reproductive biology 2004;115 Suppl 1():S80-4.
2003: S Cupisti; CM Conn; Elpida Fragouli; K Whalley; JA Mills; M J W Faed; J D A Delhanty
Sequential FISH analysis of oocytes and polar bodies reveals aneuploidy mechanisms.
Prenatal diagnosis 2003;23(8):663-8.
2003: M Simopoulou; Joyce C Harper; Elpida Fragouli; A Mantzouratou; B E Speyer; Paul Serhal; Domenico Massimo Ranieri; Alpesh Doshi; J Henderson; Charles H Rodeck; J D A Delhanty
Preimplantation genetic diagnosis of chromosome abnormalities: implications from the outcome for couples with chromosomal rearrangements.
Prenatal diagnosis 2003;23(8):652-62.
2003: J D A Delhanty
Beta thalassaemia: fetal HLA typing.
Lancet 2003;362(9377):6.
2003: Claire R Quilter; Elizabeth C Svennevik; Paul Serhal; David Ralph; Gulam Bahadur; Richard Stanhope; Marc Sütterlin; J D A Delhanty; Kay E Taylor
Cytogenetic and Y chromosome microdeletion screening of a random group of infertile males.
Fertility and sterility 2003;79(2):301-7.
2002: Claire R Quilter; NC Nathwani; Gerard S Conway; R Stanhope; David Ralph; Gulam Bahadur; Paul Serhal; K Taylor; J D A Delhanty
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: J D A Delhanty; Dagan Wells
Preimplantation genetic diagnosis: an alternative to prenatal diagnosis.
Expert review of molecular diagnostics 2002;2(5):395-9.
2002: Dagan Wells; Tomas Escudero; Brynn Levy; Kurt Hirschhorn; J D A Delhanty; Santiago Munné
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: Joyce C Harper; Dagan Wells; Wirawit Piyamongkol; Patrick M Abou-Sleiman; Angela Apessos; Antonis Ioulianos; Mary Davis; Alpesh Doshi; Paul Serhal; Massimo Ranieri; Charles Rodeck; J D A Delhanty
Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disorders.
Prenatal diagnosis 2002;22(6):525-33.
2002: Patrick M Abou-Sleiman; Angela Apessos; Joyce C Harper; Paul Serhal; Robert M L Winston; J D A Delhanty
First application of preimplantation genetic diagnosis to neurofibromatosis type 2 (NF2).
Prenatal diagnosis 2002;22(6):519-24.
2002: Anna Patrikidou; Jon Bennett; Patrick M Abou-Sleiman; J D A Delhanty; Malcolm Harris
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: Patrick M Abou-Sleiman; Angela Apessos; Joyce C Harper; Paul Serhal; J D A Delhanty
Pregnancy following preimplantation genetic diagnosis for Crouzon syndrome.
Molecular human reproduction 2002;8(3):304-9.
2002: Anna Patrikidou; Malcolm Harris; Jon Bennett; Patrick M Abou-Sleiman; J D A Delhanty
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: Wirawit Piyamongkol; Joyce C Harper; J D A Delhanty; Dagan Wells
Preimplantation genetic diagnostic protocols for alpha- and beta-thalassaemias using multiplex fluorescent PCR.
Prenatal diagnosis 2001;21(9):753-9.
2001: J D A Delhanty
Preimplantation genetics: an explanation for poor human fertility?
Annals of human genetics 2001;65(Pt 4):331-8.
2001: Angela Apessos; Patrick M Abou-Sleiman; Joyce C Harper; J D A Delhanty
Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers.
Prenatal diagnosis 2001;21(6):504-11.
2001: Wirawit Piyamongkol; Joyce C Harper; Jon K Sherlock; Alpesh Doshi; Paul Serhal; J D A Delhanty; Dagan Wells
A successful strategy for preimplantation genetic diagnosis of myotonic dystrophy using multiplex fluorescent PCR.
Prenatal diagnosis 2001;21(3):223-32.
2001: Claire R Quilter; S Holman; R M AL-Hammadi; D Theodorides; RJ Hastings; J D A Delhanty
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: Dagan Wells; J D A Delhanty
Preimplantation genetic diagnosis: applications for molecular medicine.
Trends in molecular medicine 2001;7(1):23-30.
2000: Marc Sütterlin; P A Sleiman; Elizabeth Price; Zerrin Onadim; J D A Delhanty
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: Dagan Wells; J D A Delhanty
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: J D A Delhanty; Joyce C Harper
Pre-implantation genetic diagnosis.
Baillière's best practice & research. Clinical obstetrics & gynaecology 2000;14(4):691-708.
2000: Antonis Ioulianos; Dagan Wells; Joyce C Harper; J D A Delhanty
A successful strategy for preimplantation diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.
Prenatal diagnosis 2000;20(7):593-8.
2000: P Ruangvutilert; J D A Delhanty; Paul Serhal; M Simopoulou; Charles H Rodeck; Joyce C Harper
FISH analysis on day 5 post-insemination of human arrested and blastocyst stage embryos.
Prenatal diagnosis 2000;20(7):552-60.
2000: R Mahmood; C H Brierley; M J W Faed; JA Mills; J D A Delhanty
Mechanisms of maternal aneuploidy: FISH analysis of oocytes and polar bodies in patients undergoing assisted conception.
Human genetics 2000;106(6):620-6.
2000: Joyce C Harper; J D A Delhanty
Preimplantation genetic diagnosis.
Current opinion in obstetrics & gynecology 2000;12(2):67-72.
2000: RJ Hastings; Elizabeth C Svennevik; B Setterfield; D Wells; J D A Delhanty; H Mackinnon
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: P Ruangvutilert; J D A Delhanty; Charles H Rodeck; Joyce C Harper
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: Marc Sütterlin; P A Sleiman; Zerrin Onadim; J D A Delhanty
Single cell detection of inherited retinoblastoma predisposition.
Prenatal diagnosis 1999;19(13):1231-6.
1999: Dagan Wells; Jon K Sherlock; AH Handyside; J D A Delhanty
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: J Cozzi; CM Conn; Joyce Harper; Robert M L Winston; M Rindl; P A Farndon; J D A Delhanty
A trisomic germ cell line and precocious chromatid segregation leads to recurrent trisomy 21 conception.
Human genetics 1999;104(1):23-8.
1999: CM Conn; J Cozzi; Joyce C Harper; Robert M L Winston; J D A Delhanty
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: J Harper; E Pergament; J D A Delhanty
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: Claire R Quilter; K Taylor; Gerard S Conway; NC Nathwani; J D A Delhanty
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: Asangla Ao; Dagan Wells; AH Handyside; Robert M L Winston; J D A Delhanty
Preimplantation genetic diagnosis of inherited cancer: familial adenomatous polyposis coli.
Journal of assisted reproduction and genetics 1998;15(3):140-4.
1998: CM Conn; Joyce C Harper; Robert M L Winston; J D A Delhanty
Infertile couples with Robertsonian translocations: preimplantation genetic analysis of embryos reveals chaotic cleavage divisions.
Human genetics 1998;102(1):117-23.
1997: J D A Delhanty
Chromosome analysis by FISH in human preimplantation genetics.
Human reproduction (Oxford, England) 1997;12(11 Suppl):153-5.
1997: N el-Hashemite; J D A Delhanty
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: J D A Delhanty; D Wells; Joyce C Harper
Genetic diagnosis before implantation.
BMJ (Clinical research ed.) 1997;315(7112):828-9.
1997: N el-Hashemite; Dagan Wells; J D A Delhanty
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: AH Handyside; J D A Delhanty
Preimplantation genetic diagnosis: strategies and surprises.
Trends in genetics : TIG 1997;13(7):270-5.
1997: J D A Delhanty; Joyce C Harper; Asangla Ao; AH Handyside; Robert M L Winston
Multicolour FISH detects frequent chromosomal mosaicism and chaotic division in normal preimplantation embryos from fertile patients.
Human genetics 1997;99(6):755-60.
1997: Jon K Sherlock; Ashutosh Halder; B Tutschek; J D A Delhanty; Charles Rodeck; Matteo Adinolfi
Prenatal detection of fetal aneuploidies using transcervical cell samples.
Journal of medical genetics 1997;34(4):302-5.
1997: N el-Hashemite; Mary Petrou; A S Khalifa; N M Heshmat; M S Rady; J D A Delhanty
Identification of novel Asian Indian and Japanese mutations causing beta-thalassaemia in the Egyptian population.
Human genetics 1997;99(2):271-4.
1996: R Sud; I C Talbot; J D A Delhanty
Infrequent alterations of the APC and MCC genes in gastric cancers from British patients.
British journal of cancer 1996;74(7):1104-8.
1996: N el-Hashemite; D Wells; J D A Delhanty
Preimplantation genetic diagnosis of beta-thalassaemia.
Lancet 1996;348(9027):620-1.
1996: JE Fitzgibbon; Nicholas Katsanis; D Wells; J D A Delhanty; W Vallins; David Hunt
Human guanylate kinase (GUK1): cDNA sequence, expression and chromosomal localisation.
FEBS letters 1996;385(3):185-8.
1996: Jon K Sherlock; D K Griffin; J D A Delhanty; John Parrington
Homologies between human and marmoset (Callithrix jacchus) chromosomes revealed by comparative chromosome painting.
Genomics 1996;33(2):214-9.
1996: Joyce C Harper; J D A Delhanty
Detection of chromosomal abnormalities in human preimplantation embryos using FISH.
Journal of assisted reproduction and genetics 1996;13(2):137-9.
1996: J C Harper; J D A Delhanty
FISH in Preimplantation Diagnosis.
Methods in molecular medicine 1996;5():259-68.
1996: D Wells; P Chapman; J C Landgrebe; K Tsioupra; J D A Delhanty
Four novel germline mutations of the APC gene.
Human mutation 1996;8(2):193-5.
1995: Joyce C Harper; K Dawson; J D A Delhanty; Robert M L Winston
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: JE Fitzgibbon; D Wells; A Pilz; J D A Delhanty; M Kai; H Kanoh; D Hunt
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: B Tutschek; Jon K Sherlock; Ashutosh Halder; J D A Delhanty; Charles Rodeck; Matteo Adinolfi
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: Matteo Adinolfi; Jon K Sherlock; B Tutschek; Ashutosh Halder; J D A Delhanty; Charles Rodeck
Detection of fetal cells in transcervical samples and prenatal diagnosis of chromosomal abnormalities.
Prenatal diagnosis 1995;15(10):943-9.
1995: R M al-Jehani; Sue Povey; J D A Delhanty; John Parrington
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: S A Gayther; R Sud; D Wells; K Tsioupra; J D A Delhanty
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: J D A Delhanty; A H Handyside
The origin of genetic defects in the human and their detection in the preimplantation embryo.
Human reproduction update 1995;1(3):201-15.
1995: J D A Delhanty; K Tsioupra
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: Joyce C Harper; Edith Coonen; AH Handyside; Robert M L Winston; Anton H N Hopman; J D A Delhanty
Mosaicism of autosomes and sex chromosomes in morphologically normal, monospermic preimplantation human embryos.
Prenatal diagnosis 1995;15(1):41-9.
1994: Edith Coonen; Joyce C Harper; Frans C S Ramaekers; J D A Delhanty; Anton H N Hopman; Joep P M Geraedts; AH Handyside
Presence of chromosomal mosaicism in abnormal preimplantation embryos detected by fluorescence in situ hybridisation.
Human genetics 1994;94(6):609-15.
1994: J D A Delhanty
Preimplantation diagnosis.
Prenatal diagnosis 1994;14(13):1217-27.
1994: Joyce C Harper; F Robinson; S Duffy; D K Griffin; AH Handyside; J D A Delhanty; Robert M L Winston
Detection of fertilization in embryos with accelerated cleavage by fluorescent in-situ hybridization (FISH).
Human reproduction (Oxford, England) 1994;9(9):1733-7.
1994: S F Ding; J D A Delhanty; George C Zografos; N E Michail; J S Dooley; Nagy A Habib
Chromosome allele loss in colorectal liver metastases and its association with clinical features.
The British journal of surgery 1994;81(6):875-8.
1994: S A Gayther; M Rees; J D A Delhanty
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: Joyce C Harper; Edith Coonen; Frans C S Ramaekers; J D A Delhanty; AH Handyside; Robert M L Winston; Anton H N Hopman
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: JE Fitzgibbon; Binoy Appukuttan; S Gayther; D Wells; J D A Delhanty; David Hunt
Localisation of the human blue cone pigment gene to chromosome band 7q31.3-32.
Human genetics 1994;93(1):79-80.
1994: S A Gayther; D Wells; S B SenGupta; P Chapman; K Neale; K Tsioupra; J D A Delhanty
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: JE Fitzgibbon; A Pilz; S Gayther; Binoy Appukuttan; KS Dulai; J D A Delhanty; George M Helmkamp; Lynwood R Yarbrough; David Hunt
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: J D A Delhanty; D K Griffin; AH Handyside; J Harper; G H Atkinson; M H Pieters; Robert M L Winston
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: S Gayther; D Wells; K Gulati; P Chapman; J Burn; J D A Delhanty
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: D K Griffin; L J Wilton; AH Handyside; G H Atkinson; Robert M L Winston; J D A Delhanty
Diagnosis of sex in preimplantation embryos by fluorescent in situ hybridisation.
BMJ (Clinical research ed.) 1993;306(6889):1382.
1993: M Rees; S E Leigh; J D A Delhanty; L Bowles; I C Talbot
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: S F Ding; J D A Delhanty; L Bowles; J S Dooley; C B Wood; Nagy A Habib
Loss of constitutional heterozygosity on chromosomes 5 and 17 in cholangiocarcinoma.
British journal of cancer 1993;67(5):1007-10.
1993: S F Ding; J D A Delhanty; L Bowles; J S Dooley; C B Wood; Nagy A Habib
Infrequent chromosome allele loss in fibrolamellar carcinoma.
British journal of cancer 1993;67(2):244-6.
1993: S F Ding; J D A Delhanty; J S Dooley; L Bowles; C B Wood; Nagy A Habib
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: S F Ding; R P Jalleh; C B Wood; L Bowles; J D A Delhanty; J Dooley; Nagy A Habib
Different DNA changes in primary and recurrent hepatocellular carcinoma.
Gut 1992;33(10):1433-5.
1992: S F Ding; Nagy A Habib; J D A Delhanty; L Bowles; L Greco; C Wood; Robin C N Williamson; J S Dooley
Loss of heterozygosity on chromosomes 1 and 11 in carcinoma of the pancreas.
British journal of cancer 1992;65(6):809-12.
1992: D K Griffin; L J Wilton; AH Handyside; Robert M L Winston; J D A Delhanty
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: I Cross; J D A Delhanty; P Chapman; L V Bowles; D Griffin; John Wolstenholme; M Bradburn; J Brown; C Wood; A Gunn
An intrachromosomal insertion causing 5q22 deletion and familial adenomatous polyposis coli in two generations.
Journal of medical genetics 1992;29(3):175-9.
1992: M B Cachon Gonzalez; J Wolfe; J D A Delhanty
Dinucleotide repeat polymorphism at the D5S98 locus.
Nucleic acids research 1992;20(4):924.
1991: S F Ding; Nagy A Habib; J Dooley; C Wood; L Bowles; J D A Delhanty
Loss of constitutional heterozygosity on chromosome 5q in hepatocellular carcinoma without cirrhosis.
British journal of cancer 1991;64(6):1083-7.
1991: Z Ulinowski; K Taylor; D Griffin; J D A Delhanty; Jonathan Wolfe
D12S56: a highly polymorphic locus on human chromosome 12q14.
Annals of human genetics 1991;55(Pt 4):279-82.
1991: M B Cachon-Gonzalez; J D A Delhanty; John Burn; K Tsioupra; M B Davis; J Attwood; P Chapman
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: F Florian; N Hornigold; D K Griffin; J D A Delhanty; L Sefton; C Abbott; C Jones; P N Goodfellow; Jonathan Wolfe
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: John Burn; P Chapman; J D A Delhanty; C Wood; Fiona Lalloo; M B Cachon-Gonzalez; K Tsioupra; W Church; M Rhodes; A Gunn
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: D K Griffin; AH Handyside; R J Penketh; Robert M L Winston; J D A Delhanty
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: C B Bunker; D Atherton; O P Gray; K Tsioupra; J D A Delhanty; P M Dowd
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: J D A Delhanty; R J Penketh
Cytogenetic analysis of unfertilized oocytes retrieved after treatment with the LHRH analogue, buserelin.
Human reproduction (Oxford, England) 1990;5(6):699-702.
1990: M N Khouzam; K Tsioupra; J D A Delhanty
Chromosome breakage in lymphocytes from members of cancer families showing autosomal dominant inheritance.
Clinical genetics 1990;38(1):51-6.
1990: D K Griffin; S E Leigh; J D A Delhanty
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: J D A Delhanty; H M Cooke
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: J D A Delhanty
Rapid chromosomal sexing of birds by direct and short term culture techniques.
The Veterinary record 1989;125(4):92.
1989: R J Penketh; J D A Delhanty; J A van den Berghe; E M Finklestone; AH Handyside; S Malcolm; Robert M L Winston
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: M Rees; S E Leigh; J D A Delhanty; J R Jass
Chromosome 5 allele loss in familial and sporadic colorectal adenomas.
British journal of cancer 1989;59(3):361-5.
1989: AH Handyside; J K Pattinson; R J Penketh; J D A Delhanty; Robert M L Winston; E G Tuddenham
Biopsy of human preimplantation embryos and sexing by DNA amplification.
Lancet 1989;1(8634):347-9.
1988: M A Aldred; M Rees; K Tsioupra; S E Leigh; K F Neale; J D A Delhanty
Familial polyposis coli.
Lancet 1988;2(8610):565.
1988: J D A Delhanty; John Parrington
The origin of isochromosomes.
Clinical genetics 1988;34(3):207-8.
1988: J D A Delhanty; S H Rider
Transformation studies on human fibroblasts from familial polyposis coli patients and normal donors.
Mutation research 1988;199(2):327-39.
1988: K Tsioupra; L F West; M B Davis; John Parrington; J D A Delhanty
Spontaneous and induced chromosome damage in lymphocytes of medullary thyroid carcinoma patients and their family members.
Disease markers 1988;6(2):127-32.
1988: H A Mazzullo; J Attwood; J D A Delhanty
Familial polyposis coli: no evidence for increased sensitivity to mitomycin C.
Journal of medical genetics 1988;25(4):233-7.
1986: H M Cooke; R J Penketh; J D A Delhanty
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: J D A Delhanty; John Parrington; G Casey; J Attwood; L West; D Kirk; G Corney
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.