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Peter Ray

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
13
Klamut, Henry
9
Burghes, Arthur
7
Howard, PL
7
Pillers, De-Ann
6
Weleber, Richard
5
Smith, Adam
5
Steele, Leslie
5
Stockley, Tracy
5
Weksberg, Rosanna
5
Chun, Kathy
5
Karpati, George
5
Dally, Ghassan
4
Chitayat, David
4
Austin, Richard
4
Prior, Thomas

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Publications

TOP 3
Baskin Berivan; Banwell Brenda; Khater Reem Al; Hawkins Cynthia; Ray Peter N
Becker muscular dystrophy caused by an intronic mutation reducing the efficiency of the splice donor site of intron 26 of the dystrophin gene.
Vajsar Jiri; Baskin Berivan; Swoboda Kathryn; Biggar Doug W; Schachter Harry; Ray Peter N
Walker-Warburg Syndrome with POMT1 mutations can be associated with cleft lip and cleft palate.
Stachon Andrea C; Baskin Berivan; Smith Adam C; Shugar Andrea; Cytrynbaum Cheryl; Fishman Leona; Mendoza-Londono Roberto; Klatt Regan; Teebi Ahmed; Ray Peter N; Weksberg Rosanna
Molecular diagnosis of 22q11.2 deletion and duplication by multiplex ligation dependent probe amplification.

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All Publications

2009: Baskin Berivan; Banwell Brenda; Khater Reem Al; Hawkins Cynthia; Ray Peter N
Becker muscular dystrophy caused by an intronic mutation reducing the efficiency of the splice donor site of intron 26 of the dystrophin gene.
Neuromuscular disorders : NMD 2009;19(3):189-92.
2008: Vajsar Jiri; Baskin Berivan; Swoboda Kathryn; Biggar Doug W; Schachter Harry; Ray Peter N
Walker-Warburg Syndrome with POMT1 mutations can be associated with cleft lip and cleft palate.
Neuromuscular disorders : NMD 2008;18(8):675-7.
2007: Stachon Andrea C; Baskin Berivan; Smith Adam C; Shugar Andrea; Cytrynbaum Cheryl; Fishman Leona; Mendoza-Londono Roberto; Klatt Regan; Teebi Ahmed; Ray Peter N; Weksberg Rosanna
Molecular diagnosis of 22q11.2 deletion and duplication by multiplex ligation dependent probe amplification.
American journal of medical genetics. Part A 2007;143A(24):2924-30.
2007: Smith Adam C; Shuman Cheryl; Chitayat David; Steele Leslie; Ray Peter N; Bourgeois Jaqueline; Weksberg Rosanna
Severe presentation of Beckwith-Wiedemann syndrome associated with high levels of constitutional paternal uniparental disomy for chromosome 11p15.
American journal of medical genetics. Part A 2007;143A(24):3010-5.
2006: Saengpattrachai Montri; Ray Peter N; Hawkins Cynthia E; Berzen Alan; Banwell Brenda L
Grandpa and I have dystrophinopathy?: approach to asymptomatic hyperCKemia.
Pediatric neurology 2006;35(2):145-9.
2006: Shuman Cheryl; Smith Adam C; Steele Leslie; Ray Peter N; Clericuzio Carol; Zackai Elaine; Parisi Melissa A; Meadows Anna T; Kelly Thaddeus; Tichauer David; Squire Jeremy A; Sadowski Paul; Weksberg Rosanna
Constitutional UPD for chromosome 11p15 in individuals with isolated hemihyperplasia is associated with high tumor risk and occurs following assisted reproductive technologies.
American journal of medical genetics. Part A 2006;140(14):1497-503.
2006: Stockley Tracy L; Akber Sarah; Bulgin Natalie; Ray Peter N
Strategy for comprehensive molecular testing for Duchenne and Becker muscular dystrophies.
Genetic testing 2006;10(4):229-43.
2006: Smith A C; Rubin T; Shuman C; Estabrooks L; Aylsworth A S; McDonald M T; Steele L; Ray P N; Weksberg R
New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome.
Cytogenetic and genome research 2006;113(1-4):313-7.
2005: Bishop Michele D; Freedman Steven D; Zielenski Julian; Ahmed Najma; Dupuis Annie; Martin Sheelagh; Ellis Lynda; Shea Julie; Hopper Isobel; Corey Mary; Kortan Paul; Haber Gregory; Ross Christine; Tzountzouris John; Steele Leslie; Ray Peter N; Tsui Lap-Chee; Durie Peter R
The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis.
Human genetics 2005;118(3-4):372-81.
2005: Sato Christine; Morgan Angharad; Lang Anthony E; Salehi-Rad Shabnam; Kawarai Toshitaka; Meng Yan; Ray Peter N; Farrer Lindsay A; St George-Hyslop Peter; Rogaeva Ekaterina
Analysis of the glucocerebrosidase gene in Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2005;20(3):367-70.
2004: Goos Lisa M; Silverman Irwin; Steele Leslie; Stockley Tracy; Ray Peter N
Providing information at the point of care: educational diagnostic reports from a genetic testing service provider.
Clinical leadership & management review : the journal of CLMA 2004;18(1):11-24.
2004: Feigenbaum Annette; Moore Robert; Clarke Joe; Hewson Stacy; Chitayat David; Ray Peter N; Stockley Tracy L
Canavan disease: carrier-frequency determination in the Ashkenazi Jewish population and development of a novel molecular diagnostic assay.
American journal of medical genetics. Part A 2004;124A(2):142-7.
2003: Chun Kathy; Teebi Ahmad S; Azimi Cyrus; Steele Leslie; Ray Peter N
Screening of patients with craniosynostosis: molecular strategy.
American journal of medical genetics. Part A 2003;120A(4):470-3.
2003: Cisternas Felipe A; Vincent John B; Scherer Stephen W; Ray Peter N
Cloning and characterization of human CADPS and CADPS2, new members of the Ca2+-dependent activator for secretion protein family.
Genomics 2003;81(3):279-91.
2003: Stockley Tracy L; Ray Peter N
Multiplexed fluorescence analysis for mutations causing Tay-Sachs disease.
Methods in molecular biology (Clifton, N.J.) 2003;217():131-41.
2002: Austin Richard C; Fox Joan E B; Werstuck Geoff H; Stafford Alan R; Bulman Dennis E; Dally Ghassan Y; Ackerley Cameron A; Weitz Jeffrey I; Ray Peter N
Identification of Dp71 isoforms in the platelet membrane cytoskeleton. Potential role in thrombin-mediated platelet adhesion.
The Journal of biological chemistry 2002;277(49):47106-13.
2002: Biggar W Douglas; Klamut Henry J; Demacio Paula C; Stevens Daniel J; Ray Peter N
Duchenne muscular dystrophy: current knowledge, treatment, and future prospects.
Clinical orthopaedics and related research 2002;(401):88-106.
2002: Chun Kathy; Teebi Ahmad S; Jung Jack H; Kennedy Shelley; Laframboise Rachel; Meschino Wendy S; Nakabayashi Kazuhiko; Scherer Stephen W; Ray Peter N; Teshima Ikuko
Genetic analysis of patients with the Saethre-Chotzen phenotype.
American journal of medical genetics 2002;110(2):136-43.
2002: Zeesman Susan; Whelan Donald T; Carson Nancy; McGowan-Jordan Jean; Stockley Tracy L; Ray Peter N; Prior Thomas W
Parents of children with spinal muscular atrophy are not obligate carriers: carrier testing is important for reproductive decision-making.
American journal of medical genetics 2002;107(3):247-9.
2002: Teebi Ahmad S; Kennedy Shelley; Chun Kathy; Ray Peter N
Severe and mild phenotypes in Pfeiffer syndrome with splice acceptor mutations in exon IIIc of FGFR2.
American journal of medical genetics 2002;107(1):43-7.
2001: Demacio P C; Ray P N
Alpha-catulin maps to the familial dysautonomia region on 9q31.
Genome / National Research Council Canada = Génome / Conseil national de recherches Canada 2001;44(6):990-4.
2001: Weksberg R; Nishikawa J; Caluseriu O; Fei Y L; Shuman C; Wei C; Steele L; Cameron J; Smith A; Ambus I; Li M; Ray P N; Sadowski P; Squire J
Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.
Human molecular genetics 2001;10(26):2989-3000.
2000: González E; Montañez C; Ray P N; Howard P L; García-Sierra F; Mornet D; Cisneros B
Alternative splicing regulates the nuclear or cytoplasmic localization of dystrophin Dp71.
FEBS letters 2000;482(3):209-14.
2000: Austin R C; Morris G E; Howard P L; Klamut H J; Ray P N
Expression and synthesis of alternatively spliced variants of Dp71 in adult human brain.
Neuromuscular disorders : NMD 2000;10(3):187-93.
1999: Pillers D A; Fitzgerald K M; Duncan N M; Rash S M; White R A; Dwinnell S J; Powell B R; Schnur R E; Ray P N; Cibis G W; Weleber R G
Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutations.
Human genetics 1999;105(1-2):2-9.
1999: Huggins M J; Smith J R; Chun K; Ray P N; Shah J K; Whelan D T
Achondroplasia-hypochondroplasia complex in a newborn infant.
American journal of medical genetics 1999;84(5):396-400.
1999: Pillers D A; Weleber R G; Green D G; Rash S M; Dally G Y; Howard P L; Powers M R; Hood D C; Chapman V M; Ray P N; Woodward W R
Effects of dystrophin isoforms on signal transduction through neural retina: genotype-phenotype analysis of duchenne muscular dystrophy mouse mutants.
Molecular genetics and metabolism 1999;66(2):100-10.
1999: Howard P L; Dally G Y; Ditta S D; Austin R C; Worton R G; Klamut H J; Ray P N
Dystrophin isoforms DP71 and DP427 have distinct roles in myogenic cells.
Muscle & nerve 1999;22(1):16-27.
1998: Howard P L; Klamut H J; Ray P N
Identification of a novel actin binding site within the Dp71 dystrophin isoform.
FEBS letters 1998;441(2):337-41.
1998: Vajsar J; Balslev T; Ray P N; Siegel-Bartelt J; Jay V
Congenital cytoplasmic body myopathy with survival motor neuron gene deletion or Werdnig-Hoffmann disease.
Neurology 1998;51(3):873-5.
1998: Howard P L; Dally G Y; Wong M H; Ho A; Weleber R G; Pillers D A; Ray P N
Localization of dystrophin isoform Dp71 to the inner limiting membrane of the retina suggests a unique functional contribution of Dp71 in the retina.
Human molecular genetics 1998;7(9):1385-91.
1998: Chun K; Siegel-Bartelt J; Chitayat D; Phillips J; Ray P N
FGFR2 mutation associated with clinical manifestations consistent with Antley-Bixler syndrome.
American journal of medical genetics 1998;77(3):219-24.
1998: Allingham-Hawkins D J; McGlynn-Steele L K; Brown C A; Sutherland J; Ray P N
Impact of carrier status determination for Duchenne/Becker muscular dystrophy by computer-assisted laser densitometry.
American journal of medical genetics 1998;75(2):171-5.
1998: Costa T; Lambert M; Teshima I; Ray P N; Richer C L; Dallaire L
Monozygotic twins with 45,X/46,XY mosaicism discordant for phenotypic sex.
American journal of medical genetics 1998;75(1):40-4.
1997: Rochette C F; Surh L C; Ray P N; McAndrew P E; Prior T W; Burghes A H; Vanasse M; Simard L R
Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7.
Neurogenetics 1997;1(2):141-7.
1997: Costa T; Greer W; Rysiecki G; Buncic J R; Ray P N
Monozygotic twins discordant for Aicardi syndrome.
Journal of medical genetics 1997;34(8):688-91.
1997: McAndrew P E; Parsons D W; Simard L R; Rochette C; Ray P N; Mendell J R; Prior T W; Burghes A H
Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number.
American journal of human genetics 1997;60(6):1411-22.
1997: Strasberg P M; Noreau D; McGlynn-Steele L; Koultchitski G; Ray P N
PCR-based test for two cystic fibrosis mutations (A455E, 711 + 1 G-->T) common among French Canadians.
Clinical chemistry 1997;43(6 Pt 1):1083-4.
1997: Klamut H J; Bosnoyan-Collins L O; Worton R G; Ray P N
A muscle-specific enhancer within intron 1 of the human dystrophin gene is functionally dependent on single MEF-1/E box and MEF-2/AT-rich sequence motifs.
Nucleic acids research 1997;25(8):1618-25.
1996: MacKenzie J J; Fitzpatrick J; Babyn P; Ferrero G B; Ballabio A; Billingsley G; Bulman D E; Strasberg P; Ray P N; Costa T
X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindred.
Journal of medical genetics 1996;33(10):823-8.
1996: Klamut H J; Bosnoyan-Collins L O; Worton R G; Ray P N; Davis H L
Identification of a transcriptional enhancer within muscle intron 1 of the human dystrophin gene.
Human molecular genetics 1996;5(10):1599-606.
1996: Tennyson C N; Dally G Y; Ray P N; Worton R G
Expression of the dystrophin isoform Dp71 in differentiating human fetal myogenic cultures.
Human molecular genetics 1996;5(10):1559-66.
1996: Allingham-Hawkins D J; Brown C A; Babul R; Chitayat D; Krekewich K; Humphries T; Ray P N; Teshima I E
Tissue-specific methylation differences and cognitive function in fragile X premutation females.
American journal of medical genetics 1996;64(2):329-33.
1995: Strasberg P; Liede H A; Stein T; Warren I; Sutherland J; Ray P N
A novel mutation in the Norrie disease gene predicted to disrupt the cystine knot growth factor motif.
Human molecular genetics 1995;4(11):2179-80.
1995: Austin R C; Howard P L; D'Souza V N; Klamut H J; Ray P N
Cloning and characterization of alternatively spliced isoforms of Dp71.
Human molecular genetics 1995;4(9):1475-83.
1995: Allingham-Hawkins D J; Ray P N
FRAXE expansion is not a common etiological factor among developmentally delayed males.
American journal of human genetics 1995;57(1):72-6.
1995: D'Souza V N; Nguyen T M; Morris G E; Karges W; Pillers D A; Ray P N
A novel dystrophin isoform is required for normal retinal electrophysiology.
Human molecular genetics 1995;4(5):837-42.
1995: Pillers D A; Weleber R G; Woodward W R; Green D G; Chapman V M; Ray P N
mdxCv3 mouse is a model for electroretinography of Duchenne/Becker muscular dystrophy.
Investigative ophthalmology & visual science 1995;36(2):462-6.
1994: Sigesmund D A; Weleber R G; Pillers D A; Westall C A; Panton C M; Powell B R; Héon E; Murphey W H; Musarella M A; Ray P N
Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy.
Ophthalmology 1994;101(5):856-65.
1994: Bapat B V; Parker J A; Berk T; Cohen Z; McLeod R S; Ray P N; Stern H S
Combined use of molecular and biomarkers for presymptomatic carrier risk assessment in familial adenomatous polyposis: implications for screening guidelines.
Diseases of the colon and rectum 1994;37(2):165-71.
1993: Pillers D A; Seltzer W K; Powell B R; Ray P N; Tremblay F; La Roche G R; Lewis R A; McCabe E R; Eriksson A W; Weleber R G
Negative-configuration electroretinogram in Oregon eye disease. Consistent phenotype in Xp21 deletion syndrome.
Archives of ophthalmology 1993;111(11):1558-63.
1993: Winnard A V; Klein C J; Coovert D D; Prior T; Papp A; Snyder P; Bulman D E; Ray P N; McAndrew P; King W
Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophy.
Human molecular genetics 1993;2(6):737-44.
1993: Bebchuk K G; Bulman D E; D'Souza V N; Worton R G; Ray P N
Genomic organization of exons 22 to 25 of the dystrophin gene.
Human molecular genetics 1993;2(5):593-4.
1992: Gangopadhyay S B; Sherratt T G; Heckmatt J Z; Dubowitz V; Miller G; Shokeir M; Ray P N; Strong P N; Worton R G
Dystrophin in frameshift deletion patients with Becker muscular dystrophy.
American journal of human genetics 1992;51(3):562-70.
1992: Wijmenga C; Sandkuijl L A; Moerer P; van der Boorn N; Bodrug S E; Ray P N; Brouwer O F; Murray J C; van Ommen G J; Padberg G W
Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter.
American journal of human genetics 1992;51(2):411-5.
1992: Clarke J T; Wilson P J; Morris C P; Hopwood J J; Richards R I; Sutherland G R; Ray P N
Characterization of a deletion at Xq27-q28 associated with unbalanced inactivation of the nonmutant X chromosome.
American journal of human genetics 1992;51(2):316-22.
1992: Klein C J; Coovert D D; Bulman D E; Ray P N; Mendell J R; Burghes A H
Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibers.
American journal of human genetics 1992;50(5):950-9.
1992: Hu X; Bulman D E; Ray P N; Worton R G
Frameshift duplication resulting in truncated dystrophin in a patient with Duchenne muscular dystrophy.
Human mutation 1992;1(2):172-3.
1991: Bodrug S E; Holden J J; Ray P N; Worton R G
Molecular analysis of X-autosome translocations in females with Duchenne muscular dystrophy.
The EMBO journal 1991;10(12):3931-9.
1991: Hu X Y; Ray P N; Worton R G
Mechanisms of tandem duplication in the Duchenne muscular dystrophy gene include both homologous and nonhomologous intrachromosomal recombination.
The EMBO journal 1991;10(9):2471-7.
1991: Bapat B; Groffen J; Ray P N
The human tyrosine kinase gene (FER) detects an RFLP with BgII.
Nucleic acids research 1991;19(15):4310.
1991: Clarke J T; Greer W L; Strasberg P M; Pearce R D; Skomorowski M A; Ray P N
Hunter disease (mucopolysaccharidosis type II) associated with unbalanced inactivation of the X chromosomes in a karyotypically normal girl.
American journal of human genetics 1991;49(2):289-97.
1991: Bulman D E; Gangopadhyay S B; Bebchuck K G; Worton R G; Ray P N
Point mutation in the human dystrophin gene: identification through western blot analysis.
Genomics 1991;10(2):457-60.
1991: Bulman D E; Murphy E G; Zubrzycka-Gaarn E E; Worton R G; Ray P N
Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific for dystrophin.
American journal of human genetics 1991;48(2):295-304.
1991: Bapat B; Bei X; Mahuran D; Ray P N
Two polymorphisms for the human GM2 activator protein gene.
Nucleic acids research 1991;19(3):683.
1991: Zubrzycka-Gaarn E E; Hutter O F; Karpati G; Klamut H J; Bulman D E; Hodges R S; Worton R G; Ray P N
Dystrophin is tightly associated with the sarcolemma of mammalian skeletal muscle fibers.
Experimental cell research 1991;192(1):278-88.
1991: Langley J M; Balfe J W; Selander T; Ray P N; Clarke J T
Autosomal recessive inheritance of vasopressin-resistant diabetes insipidus.
American journal of medical genetics 1991;38(1):90-4.
1991: Cullen M J; Walsh J; Nicholson L V; Harris J B; Zubrzycka-Gaarn E E; Ray P N; Worton R G
Immunogold labelling of dystrophin in human muscle, using an antibody to the last 17 amino acids of the C-terminus.
Neuromuscular disorders : NMD 1991;1(2):113-9.
1990: Taylor R G; Lambert M A; Sexsmith E; Sadler S J; Ray P N; Mahuran D J; McInnes R R
Cloning and expression of rat histidase. Homology to two bacterial histidases and four phenylalanine ammonia-lyases.
The Journal of biological chemistry 1990;265(30):18192-9.
1990: Bodrug S E; Roberson J R; Weiss L; Ray P N; Worton R G; Van Dyke D L
Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.
Journal of medical genetics 1990;27(7):426-32.
1990: Carpenter S; Karpati G; Zubrzycka-Gaarn E; Bulman D E; Ray P N; Worton R G
Dystrophin is localized to the plasma membrane of human skeletal muscle fibers by electron-microscopic cytochemical study.
Muscle & nerve 1990;13(5):376-80.
1990: Hu X Y; Ray P N; Murphy E G; Thompson M W; Worton R G
Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotypegenotype correlation.
American journal of human genetics 1990;46(4):682-95.
1990: Karpati G; Zubrzycka-Gaarn E E; Carpenter S; Bulman D E; Ray P N; Worton R G
Age-related conversion of dystrophin-negative to -positive fiber segments of skeletal but not cardiac muscle fibers in heterozygote mdx mice.
Journal of neuropathology and experimental neurology 1990;49(2):96-105.
1990: Klamut H J; Gangopadhyay S B; Worton R G; Ray P N
Molecular and functional analysis of the muscle-specific promoter region of the Duchenne muscular dystrophy gene.
Molecular and cellular biology 1990;10(1):193-205.
1990: Worton R G; Bulman D E; Zubrzycka-Gaarn E E; Ray P N
Genetic and biochemical determinations in the pre-transplant workup and in the post-transplant assessment period.
Advances in experimental medicine and biology 1990;280():219-25; discussion 225-6.
1990: Ray P N; Klamut H J; Worton R G
The DMD gene promoter: a potential role in gene therapy.
Advances in experimental medicine and biology 1990;280():107-11; discussion 111-2.
1989: Klamut H J; Zubrzycka-Gaarn E E; Bulman D E; Malhotra S B; Bodrug S E; Worton R G; Ray P N
Myogenic regulation of dystrophin gene expression.
British medical bulletin 1989;45(3):681-702.
1989: Karpati G; Pouliot Y; Zubrzycka-Gaarn E; Carpenter S; Ray P N; Worton R G; Holland P
Dystrophin is expressed in mdx skeletal muscle fibers after normal myoblast implantation.
The American journal of pathology 1989;135(1):27-32.
1989: Hu X Y; Burghes A H; Bulman D E; Ray P N; Worton R G
Evidence for mutation by unequal sister chromatid exchange in the Duchenne muscular dystrophy gene.
American journal of human genetics 1989;44(6):855-63.
1989: Zhang Y P; Lambert M A; Cairney A E; Wills D; Ray P N; Andrulis I L
Molecular structure of the human asparagine synthetase gene.
Genomics 1989;4(3):259-65.
1988: Malhotra S B; Hart K A; Klamut H J; Thomas N S; Bodrug S E; Burghes A H; Bobrow M; Harper P S; Thompson M W; Ray P N
Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy.
Science (New York, N.Y.) 1988;242(4879):755-9.
1988: Cox D W; Wills D E; Quan F; Ray P N
A deletion of one nucleotide results in functional deficiency of apolipoprotein CII (apo CII Toronto).
Journal of medical genetics 1988;25(10):649-52.
1988: Hu X Y; Burghes A H; Ray P N; Thompson M W; Murphy E G; Worton R G
Partial gene duplication in Duchenne and Becker muscular dystrophies.
Journal of medical genetics 1988;25(6):369-76.
1988: Zubrzycka-Gaarn E E; Bulman D E; Karpati G; Burghes A H; Belfall B; Klamut H J; Talbot J; Hodges R S; Ray P N; Worton R G
The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle.
Nature 1988;333(6172):466-9.
1988: Worton R G; Ray P N; Bodrug S; Burghes A H; Hu X; Thompson M W
The problem of Duchenne muscular dystrophy.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences 1988;319(1194):275-84.
1988: Worton R G; Sutherland J; Sylvester J E; Willard H F; Bodrug S; Dubé I; Duff C; Kean V; Ray P N; Schmickel R D
Human ribosomal RNA genes: orientation of the tandem array and conservation of the 5' end.
Science (New York, N.Y.) 1988;239(4835):64-8.
1987: Bodrug S E; Ray P N; Gonzalez I L; Schmickel R D; Sylvester J E; Worton R G
Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophy.
Science (New York, N.Y.) 1987;237(4822):1620-4.
1987: Burghes A H; Logan C; Hu X; Belfall B; Worton R G; Ray P N
A cDNA clone from the Duchenne/Becker muscular dystrophy gene.
Nature 1987;328(6129):434-7.
1986: Thompson M W; Ray P N; Belfall B; Duff C; Logan C; Oss I; Worton R G
Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy.
Journal of medical genetics 1986;23(6):548-55.
1986: Kean V M; Macleod H L; Thompson M W; Ray P N; Verellen-Dumoulin C; Worton R G
Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy.
Journal of medical genetics 1986;23(6):491-3.
1986: Lambert M A; Simard L R; Ray P N; McInnes R R
Molecular cloning of cDNA for rat argininosuccinate lyase and its expression in rat hepatoma cell lines.
Molecular and cellular biology 1986;6(5):1722-8.
1986: Worton R G; Ray P N; Bodrug S; Thompson M W
Analysis of an X-autosome translocation responsible for X-linked muscular dystrophy.
Cold Spring Harbor symposia on quantitative biology 1986;51 Pt 1():345-8.
1985: Ray P N; Belfall B; Duff C; Logan C; Kean V; Thompson M W; Sylvester J E; Gorski J L; Schmickel R D; Worton R G
Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.
Nature 1985;318(6047):672-5.

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