Fragile X leads to X chromosome loss: Comments from a cytogeneticist von Duncan, Alessandra M.V.

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Human microphthalmia associated with mutations in the retinal homeobox gene CHX10 von Sarfarazi, Mansoor, McInnes, Roderick R, Ferda Percin, E, Ploder, Lynda A, Yu, Jessica J, Arici, Kemal, Jonathan Horsford, D, Rutherford, Adam, Bapat, Bharati, Cox, Diane W, Duncan, Alessandra M.V, Kalnins, Vitauts I, Kocak-Altintas, Aysegul, Sowden, Jane C, Traboulsi, Elias

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Use of array genomic hybridization technology for constitutional genetic diagnosis in Canada von Duncan, Alessandra MV, Chodirker, Bernard

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Locus-specific dual color-probe for the enumeration of chromosome 18 in rapid FISH aneuploidy testing on uncultured amniocytes von Soucy, Jean-François, Lavoie, Josée, Duncan, Alessandra M. V.

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Regulation of cisplatin resistance and homologous recombinational repair by the TFIIH subunit XPD von ALOYZ, Raquel, XU, Zhi-Yuan, BELLO, Vanessa, BERGERON, Josée, HAN, Fei-Yu, YIFEI YAN, MALAPETSA, Areti, ALAOUI-JAMALI, Moulay A, DUNCAN, Alessandra M. V, PANASCI, Lawrence

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Use of a DNA Method, QF-PCR, in the Prenatal Diagnosis of Fetal Aneuploidies von Langlois, Sylvie, MD, Duncan, Alessandra, PhD, Wilson, R. Douglas, MD, Audibert, François, MD, Brock, Jo-Ann, MD, Carroll, June, MD, Cartier, Lola, MSc, CCGC, Désilets, Valérie A., MD, Gagnon, Alain, MD, Johnson, Jo-Ann, MD, Murphy-Kaulbeck, Lynn, MD, Okun, Nanette, MD, Pastuck, Melanie, RN, Chitayat, David, MD, DeBie, Isabelle, MD, Demczuk, Suzanne, PhD, Geraghty, Michael T., MD, Marcadier, Janet, MSc, Nelson, Tanya N., PhD, Siu, Vicky, MD, Skidmore, David, MD

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Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification von Goyette, Philippe, Sumner, James S, Milos, Renate, Duncan, Alessandra M.V, Rosenblatt, David S, Matthews, Rowena G, Rozen, Rima

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Prenatal cytogenetic assessment and inv(2)(p11.2q13) von Hysert, Meaghan, Bruyère, Hélène, Côté, Gilbert B., Dawson, Angelika J., Dolling, Jo-Anna, Fetni, Raouf, Hrynchak, Monica, Lavoie, Josée, McGowan-Jordan, Jean, Tihy, Frédérique, Duncan, Alessandra M. V.

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Complete DiGeorge Anomaly in the Absence of Neonatal Hypocalcemia and Velofacial and Cardiac Defects von Al-Tamemi, Salem, Mazer, Bruce, Mitchell, David, Albuquerque, Pedro, Duncan, Alessandra M. V, McCusker, Christine, Jabado, Nada

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Use of Array Genomic Hybridization Technology in Prenatal Diagnosis in Canada von Duncan, Alessandra, PhD, Langlois, Sylvie, MD, Wilson, R. Douglas, MD, Audibert, François, MD, Brock, Jo-Ann, MD, Carroll, June, MD, Cartier, Lola, MSc, CCGC, Gagnon, Alain, MD, Johnson, Jo-Ann, MD, Murphy-Kaulbeck, Lynn, MD, Okun, Nanette, MD, Pastuck, Melanie, RN, Chitayat, David, MD, DeBie, Isabelle, MD, Demczuk, Suzanne, PhD, Désilets, Valérie A., MD, Geraghty, Michael T., MD, Marcadier, Janet, MSc, Nelson, Tanya N., PhD, Siu, Vicky, MD, Skidmore, David, MD

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A fragile site at 10q23 (FRA10A) in a phenytoin-exposed fetus: a case report and review of the literature von Morel, Chantal F., Duncan, Alessandra M. V., Désilets, Valérie

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Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9 von Strathdee, Craig A, Duncan, Alessandra M.V, Buchwald, Manuel

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The importance of investigating an apparently simple Yq deletion detected prenatally von Thomas, Mary Ann, Desilets, Valerie, Halal, F., Duncan, Alessandra M. V.

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Lissencephaly with der(17)t(17;20)(p13.3;p12.2)mat von Thomas, Mary Ann, Duncan, Alessandra M.V., Bardin, Claudette, Kaloustian, Vazken M. Der

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Cloning and characterization of human PREB; a gene that maps to a genomic region associated with trisomy 2p syndrome von Taylor Clelland, Catherine L, Levy, Brynn, McKie, Judith M, Duncan, Alessandra M.V, Hirschhorn, Kurt, Bancroft, Carter

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Stable non-Robertsonian dicentric chromosomes: four new cases and a review von LEMYRE, EMMANUELLE, KALOUSTIAN, VAZKEN M DER, DUNCAN, ALESSANDRA M V

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PHR1 Encodes an Abundant, Pleckstrin Homology Domain-containing Integral Membrane Protein in the Photoreceptor Outer Segments von Xu, S, Ladak, R, Swanson, D A, Soltyk, A, Sun, H, Ploder, L, Vidgen, D, Duncan, A M, Garami, E, Valle, D, McInnes, R R

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Recours à une méthode ADN (QF-PCR) dans le diagnostic prénatal des aneuploïdies fœtales von Langlois, Sylvie, MD, Duncan, Alessandra, PhD, Wilson, R. Douglas, MD, Audibert, François, MD, Brock, Jo-Ann, MD, Carroll, June, MD, Cartier, Lola, MSc, CCGC, Désilets, Valérie A., MD, Gagnon, Alain, MD, Johnson, Jo-Ann, MD, Murphy-Kaulbeck, Lynn, MD, Okun, Nanette, MD, Pastuck, Melanie, inf. aut, Chitayat, David, MD, DeBie, Isabelle, MD, Demczuk, Suzanne, PhD, Geraghty, Michael T, MD, Marcadier, Janet, MSc, Nelson, Tanya N., PhD, Siu, Vicky, MD, Skidmore, David, MD

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Characterization of the Supernumerary Chromosome in Cat Eye Syndrome von McDermid, Heather E., Alessandra M. V. Duncan, Brasch, Klaus R., Jeannette J. A. Holden, Magenis, Ellen, Sheehy, Robert, Burn, John, Kardon, Nataline, Noel, Bernard, Schinzel, Albert, Teshima, Ikuko, White, Bradley N.

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Recours à la technologie d’hybridation génomique matricielle dans le cadre du diagnostic prénatal au Canada von Duncan, Alessandra, PhD, Langlois, Sylvie, MD, Wilson, R. Douglas, MD, Audibert, François, MD, Brock, Jo-Ann, MD, Carroll, June, MD, Cartier, Lola, MSc, CCGC, Gagnon, Alain, MD, Johnson, Jo-Ann, MD, Murphy-Kaulbeck, Lynn, MD, Okun, Nanette, MD, Pastuck, Melanie, Chitayat, David, MD, DeBie, Isabelle, MD, Demczuk, Suzanne, PhD, Désilets, Valérie A., MD, Geraghty, Michael T., MD, Marcadier, Janet, MSc, Nelson, Tanya N., PhD, Siu, Vicky, MD, Skidmore, David, MD

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