A. Duncan

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3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL): cloning and characterization of a mouse liver HL cDNA and subchromosomal mapping of the human and mouse HL genes

J. Nadeau, K. Schappert, E. Ziętkiewicz, 2004, Mammalian Genome.

Characterization of a small supernumerary ring X chromosome by fluorescence in situ hybridization.

H. Willard, C. Brown, A. Duncan, 1993, American journal of medical genetics.

Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage

K. Kidd, J. Kidd, P. Goodfellow, 1987, Nature.

Protein-tyrosine phosphatase SH-PTP2 (PTPN11) is localized to 12q24.1–24.3

A. Duncan, F. Jirik, U. Dechert, 1995, Human Genetics.

Lissencephaly with der(17)t(17;20)(p13.3;p12.2)mat

A. Duncan, Mary Ann Thomas, C. Bardin, 2004, American journal of medical genetics. Part A.

Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.

Carolyn J. Brown, S. Schwartz, U. Surti, 1994, American journal of human genetics.

Assignment of the endothelial-specific protein receptor tyrosine kinase gene (TEK) to human chromosome 9p21.

A. Duncan, D. Dumont, M. Breitman, 1994, Genomics.

Localization and linkage of three polymorphic DNA sequences on human chromosome 20.

K. Kidd, J. Kidd, P. Goodfellow, 1987, Cytogenetics and cell genetics.

Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A.

K. Kidd, P. Goodfellow, N. Simpson, 1985, American journal of human genetics.

Chromosomal localization of the human liver form cytochrome c oxidase subunit VIIa gene.

J. Rommens, A. Duncan, G. Mitchell, 1997, Genome.

Additional case of de novo interstitial deletion del(17)(q21.3q23) and expansion of the phenotype

A. Duncan, P. Macleod, M. Khalifa, 1993, Clinical genetics.

Cytogenetic and radiation hybrid mapping of human arachidonate 5-lipoxygenase-activating protein (ALOX5AP) to chromosome 13q12.

J. Drazen, C. Yandava, B. Kennedy, 1999, Genomics.

Xp21/autosome translocations

A. Duncan, P. Macleod, J. Holden, 1986, Clinical genetics.

Characterization of the supernumerary chromosome in cat eye syndrome.

H. McDermid, J. Burn, A. Duncan, 1986, Science.

Enhanced sensitivity of lymphoblastoid cells from individuals carrying the mutation for the fragile X syndrome to the clastogenic effects of FUdR.

A. Duncan, 1986, Mutation research.

Isolation and characterization of an α-satellite repeated sequence from human chromosome 22

J. Hamerton, H. McDermid, A. Duncan, 2004, Chromosoma.

Chromosomal localization of the gene for a human galactosyltransferase (GT-1).

T. Rutherford, A. Duncan, D. McCorquodale, 1986, Biochemical and biophysical research communications.

The frequency and distribution of apoptosis induced by three non-carcinogenic agents in mouse colonic crypts.

A. Duncan, J. Heddle, 1984, Cancer letters.

Diurnal variation in the response of gamma-ray-induced apoptosis in the mouse intestinal epithelium.

A. Duncan, A. Ronen, D. Blakey, 1983, Cancer letters.

Human mitochondrial HMG CoA synthase: liver cDNA and partial genomic cloning, chromosome mapping to 1p12-p13, and possible role in vertebrate evolution.

D. Labuda, K. Schappert, A. Duncan, 1994, Genomics.

Cloning, characterization, and chromosomal localization of human liver form cytochrome c oxidase subunit VIa related genes.

A. Duncan, B. Robinson, C. Duff, 1997, Genome.

Succinyl CoA: 3-oxoacid CoA transferase (SCOT): human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient.

C. Pérez-Cerdá, M. Ugarte, A. Duncan, 1996, American journal of human genetics.

A widely distributed putative mammalian transcriptional regulator containing multiple paired amphipathic helices, with similarity to yeast SIN3.

R. Schlegel, A. Duncan, F. Jirik, 1995, Genomics.

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) required for maintenance of the mammalian photoreceptor.

S. Scherer, L. Tsui, S. Jacobson, 1997 .

Cone-Rod Dystrophy Due to Mutations in a Novel Photoreceptor-Specific Homeobox Gene ( CRX ) Essential for Maintenance of the Photoreceptor

Stephen W Scherer, Cheryl Y Gregory-Evans, James Bellingham, 1997, Cell.

Assignment of the gene for the cytochrome c1 subunit of the mitochondrial cytochrome bc1 complex (CYC1) to human chromosome 8q24.3.

R. Rozen, A. Duncan, T. Ozawa, 1994, Genomics.

Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line.

A. Duncan, S. Cole, C. Grant, 1992, Science.

Regulation of cisplatin resistance and homologous recombinational repair by the TFIIH subunit XPD.

A. Duncan, L. Panasci, M. Alaoui-Jamali, 2002, Cancer research.

Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9

M. Buchwald, A. Duncan, C. Strathdee, 1992, Nature Genetics.

The human mitochondrial elongation factor tu (EF-Tu) gene: cDNA sequence, genomic localization, genomic structure, and identification of a pseudogene.

A. Duncan, B. Robinson, C. Duff, 1997, Gene.

Molecular characterization of the marker chromosome associated with cat eye syndrome.

B. Emanuel, M. Budarf, H. McDermid, 1994, American journal of human genetics.

Amplification of CFTR exon 9 sequences to multiple locations in the human genome.

H. Heng, L. Tsui, J. Rommens, 1997, Genomics.

Mechanism of induction of nuclear anomalies by gamma-radiation in the colonic epithelium of the mouse.

A. Duncan, J. Heddle, D. Blakey, 1985, Cancer research.

Detection of nuclear anomalies in the colonic epithelium of the mouse.

W. R. Bruce, M. Wargovich, A. Duncan, 1985, Cancer research.

Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

R. Matthews, R. Milos, R. Rozen, 1994, Nature Genetics.

Characterization of a cosmid library from flow-sorted chromosomes 11

J. Longmire, L. Deaven, O. Riess, 1994, Chromosome Research.

Trisomy 22 in a newborn with multiple malformations

A. Duncan, W. Schempp, I. Voiculescu, 1987, Human Genetics.

Phenotypic manifestation in a child with 46,X,der(X)t(X;1)(q24;q31.1).

J. Ortenberg, A. Duncan, V. D. Der Kaloustian, 2000, American journal of medical genetics.

Chromosome content and ultrastructure of radiation-induced micronuclei.

A. Duncan, J. A. Walker, D. Boreham, 1996, Mutagenesis.

Cat-eye syndrome with different marker chromosomes in a mother and daughter.

W. Sanger, A. Duncan, M. Lubinsky, 1987, American journal of medical genetics.

Reply to letter to the editor by Willatt—“Partial trisomy of 2p and neuroblastoma”

E. Lemyre, A. Duncan, M. Al-Saffar, 2001 .

Phenotype of a patient with pure partial trisomy 2p(p23-->pter).

E. Lemyre, A. Duncan, M. Al-Saffar, 2000, American journal of medical genetics.

A report of recurrent anencephaly with trisomy 2p23‐2pter: additional evidence for the involvement of 2p24 in neural tube development and evaluation of the role for cytogenetic analysis

A. Duncan, M. Khalifa, S. Winsor, 1997, Prenatal diagnosis.

Pallister-Killian syndrome: a mild case diagnosed by fluorescence in situ hybridization. Review of the literature and expansion of the phenotype.

A. Duncan, M. Bielanska, M. Khalifa, 1996, American journal of medical genetics.

Methylation of HpaII site at the human DXS16 locus on Xp22 as an assay for abnormal patterns of X inactivation.

A. Duncan, K. Harrison, M. Khalifa, 2001, American journal of medical genetics.

Stable non-Robertsonian dicentric chromosomes: four new cases and a review

E. Lemyre, A. Duncan, V. Kaloustian, 2001, Journal of medical genetics.

Refined sublocalization of the human gene encoding the beta subunit of the S100 protein (S100B) and confirmation of a subtle t(9;21) translocation using in situ hybridization.

J. Higgins, A. Duncan, R. Dunn, 1989, Cytogenetics and cell genetics.

Molecular cloning of the cDNA and chromosomal localization of the gene for a putative seven-transmembrane segment (7-TMS) receptor isolated from human spleen.

Allen D. Delaney, A. Delaney, K. Schappert, 1993, Genomics.

A polymorphic locus, D10S5, at 10q21.1

J. J. A. Holden, H. E. McDermid, P. J. Goodfellow, 1987, Nucleic Acids Res..

Assignment of the human UDP glucuronosyltransferase gene (UGT1A1) to chromosome region 2q37.

P. Bosma, A. Duncan, P. Jansen, 1993, Cytogenetics and cell genetics.

Isolation and characterization of an alpha-satellite repeated sequence from human chromosome 22.

J. Hamerton, H. McDermid, A. Duncan, 1986, Chromosoma.

Breakpoint localization of the marker chromosome associated with the cat eye syndrome.

H. McDermid, A. Duncan, B. White, 1986, American journal of human genetics.

Assignment of human glutaryl-CoA dehydrogenase gene (GCDH) to the short arm of chromosome 19 (19p13.2) by in situ hybridization and somatic cell hybrid analysis.

A. Duncan, C. Greenberg, S. Goodman, 1994, Genomics.

Interstitial 6q duplication in an adult male without growth delay or severe mental retardation.

A. Duncan, M. Khalifa, S. L. Cappon, 2000, Medical science monitor : international medical journal of experimental and clinical research.

Neurofibromatosis in a man with a ring 22: in situ hybridization studies.

A. Duncan, M. Partington, D. Soudek, 1987, Cancer genetics and cytogenetics.

Erratum: Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

R. Matthews, R. Milos, P. Goyette, 1994, Nature Genetics.

A female with monosomy 18 mosaicism: a previously undescribed chromosome abnormality

Aryn Martin, A. Duncan, M. Khalifa, 1996, Clinical genetics.

In situ hybridization studies using a molecular probe that maps to Xq27–Xq28

A. Duncan, C. Morgan, 1990, Human Genetics.

Re-evaluation of the sublocalization of esterase D and its relation to the retinoblastoma locus by in situ hybridization.

B. Gallie, J. Squire, A. Duncan, 1987, Cytogenetics and cell genetics.

Assignment of the gene (UQCRFS1) for the Rieske iron-sulfur protein subunit of the mitochondrial cytochrome bc1 complex to the 22q13 and 19q12-q13.1 regions of the human genome.

R. Rozen, A. Duncan, T. Ozawa, 1994, Genomics.

Assignment of the gene for the core protein II (UQCRC2) subunit of the mitochondrial cytochrome bc1 complex to human chromosome 16p12.

R. Rozen, A. Duncan, T. Ozawa, 1993, Genomics.

Complete DiGeorge Anomaly in the Absence of Neonatal Hypocalcemia and Velofacial and Cardiac Defects

N. Jabado, A. Duncan, B. Mazer, 2005, Pediatrics.

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10

R. Mcinnes, A. Duncan, E. Percin, 2000, Nature Genetics.

Assignment of the PSST subunit gene of human mitochondrial complex I to chromosome 19p13.

A. Duncan, B. Robinson, S. Hyslop, 1996, Genomics.

Chromosomal localization of the human gene encoding the 51-kDa subunit of mitochondrial complex I (NDUFV1) to 11q13.

H. Heng, L. Tsui, K. Schappert, 1993, Genomics.

The gene for receptor-like protein tyrosine phosphatase (PTPRB) is assigned to chromosome 12q15-->q21.

A. Duncan, F. Jirik, K. Harder, 1992, Cytogenetics and cell genetics.

SITE SPECIFICITY IN THE INDUCTION OF NUCLEAR ANOMALIES BY CARCINOGENS

A. Duncan, A. Ronen, John A. Heddle, 1983 .

Autoradiographic assay of mutants resistant to diphtheria toxin in mammalian cells in vitro.

A. Duncan, J. Heddle, A. Ronen, 1984, Proceedings of the National Academy of Sciences of the United States of America.

Evidence that skewed X inactivation is not needed for the phenotypic expression of Aicardi syndrome

A. Duncan, S. Taylor, H. Hoag, 1997, Human Genetics.

Regional localization of loci on chromosome 14 using somatic cell hybrids.

K. Grzeschik, P. Goodfellow, A. Duncan, 1994, Cytogenetics and Cell Genetics.

The E subunit of vacuolar H(+)-ATPase localizes close to the centromere on human chromosome 22.

V. Lamour, M. Lipinski, H. McDermid, 1994, Human molecular genetics.

In situ hybridization to human chromosome 1 of a cDNA probe for the gene encoding the basement membrane heparan sulfate proteoglycan (HSPG).

D. Noonan, A. Duncan, R. Wintle, 1990, Cytogenetics and Cell Genetics.

Locus‐specific dual color‐probe for the enumeration of chromosome 18 in rapid FISH aneuploidy testing on uncultured amniocytes

A. Duncan, J. Soucy, J. Lavoie, 2010, Prenatal diagnosis.

Physical and transcription map in the region 14q24.3: identification of six novel transcripts.

J. Rommens, A. Duncan, A. Roux, 1997, Genomics.

ICA1 encoding p69, a protein linked to the development of type 1 diabetes, maps to human chromosome 7p22.

A. Duncan, B. Robinson, H. Dosch, 1994, Cytogenetics and cell genetics.

The adenovirus E1A-associated 130-kD protein is encoded by a member of the retinoblastoma gene family and physically interacts with cyclins A and E.

A. Duncan, Yun Li, Y. Li, 1993, Genes & development.

Succinyl-CoA:3-oxoacid transferase (SCOT): Human cDNA and genomic cloning and chromosomal mapping of the human gene

A. Duncan, G. Mitchell, S. Kassovska‐Bratinova, 1994 .

In situ hybridization of two cloned chromosome 7 sequences tightly linked to the cystic fibrosis locus.

L. Tsui, A. Duncan, M. Buchwald, 1988, Cytogenetics and Cell Genetics.

Chromosomal localization of the human prostanoid receptor gene family.

M. Abramovitz, A. Duncan, C. Funk, 1995, Genomics.

Absence of chromosomal instability in one kindred with multiple endocrine neoplasia type 2A.

A. Duncan, C. Greenberg, 1986, Cancer genetics and cytogenetics.

Localization of the human 75-kDal Fe-S protein of NADH-coenzyme Q reductase gene (NDUFS1) to 2q33----q34.

A. Duncan, B. Robinson, W. Chow, 1992, Cytogenetics and Cell Genetics.

Mapping of the human NMDA receptor subunit (NMDAR1) and the proposed NMDA receptor glutamate-binding subunit (NMDARA1) to chromosomes 9q34.3 and chromosome 8, respectively.

C. Collins, M. Hayden, A. Duncan, 1993, Genomics.

The human protein-tyrosine phosphatase PTPα/LRP gene (PTPA) is assigned to chromosome 20p13

A. Duncan, F. Jirik, L. Anderson, 1992 .