Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II von Lamb, Neil E, Freeman, Sallie B, Savage-Austin, Amanda, Pettay, Dorothy, Taft, Lisa, Hersey, Jane, Gu, Yuanchao, Shen, Joe, Saker, Denise, May, Kristen M, Avramopoulos, Dimitris, Petersen, Michael B, Hallberg, Anni, Mikkelsen, Margareta, Hassold, Terry J, Sherman, Stephanie L

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Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination von Sherman, Stephanie L., Petersen, Michael B., Freeman, Sallie B., Hersey, Jane, Pettay, Dorothy, Taft, Lisa, Frantzen, Merete, Mikkelsen, Margareta, Hassold, Terry J.

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Risks of leukaemia and solid tumours in individuals with Down's syndrome von Hasle, Henrik, Clemmensen, Inge Haunstrup, Mikkelsen, Margareta

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Paternal nondisjunction in trisomy 21: excess of male patients von Patersen, Michael B., Antonarakis, Stylianos E., Hassold, Terry J., Freeman, Sallle B., Sherman, Stephanie L., Avramopoulos, Dimitrios, Mikkelsen, Margareta

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The G Syndrome von Pedersen, Inger Leer, Mikkelsen, Margareta, Øster, Jakob

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Investigating the Impact of the Down Syndrome Related Common MTHFR 677C>T Polymorphism in the Danish Population von Kokotas, Haris, Grigoriadou, Maria, Mikkelsen, Margareta, Giannoulia-Karantana, Aglaia, Petersen, Michael B.

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Investigating the impact of the Down syndrome related common MTHFR 677C>T polymorphism in the Danish population von Kokotas, Haris, Grigoriadou, Maria, Mikkelsen, Margareta, Giannoulia-Karantana, Aglaia, Petersen, Michael B

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Characterization of Susceptible Chiasma Configurations that Increase the Risk for Maternal Nondisjunction of Chromosome 21 von Lamb, Neil E., Feingold, Eleanor, Savage, Amanda, Avramopoulos, Dimitris, Freeman, Sallie, Gu, Yuanchao, Hallberg, Anni, Hersey, Jane, Karadima, Georgia, Pettay, Dorothy, Saker, Denise, Shen, Joe, Taft, Lisa, Mikkelsen, Margareta, Petersen, Michael B., Hassold, Terry, Sherman, Stephanie L.

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Nondisjunction in trisomy 21: Origin and mechanisms von Petersen, M.B., Mikkelsen, M.

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An (11;21) Translocation in Four Generations with Chromosome 11 Abnormalities in the Offspring von Jacobsen, Petrea, Hauge, M., Henningsen, K., Hobolth, N., Mikkelsen, Margareta, Philip, J.

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The Incidence of Down's Syndrome and Progress Towards Its Reduction [and Discussion] von Mikkelsen, Margareta, Mittwoch, Ursula, Emery, A. E. H.

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Non-Disjunction of Chromosome 18 von Bugge, Merete, Collins, Andrew, Petersen, Michael B., Fisher, Julia, Brandt, Carsten, Michael Hertz, Jens, Tranebjaerg, Lisbeth, de Lozier-Blanchet, Celia, Nicolaides, Peter, Brøndum-Nielsen, Karen, Morton, Newton, Mikkelsen, Margareta

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Elucidating the Mechanisms of Paternal Non-Disjunction of Chromosome 21 in Humans von Savage, Amanda R., Petersen, Michael B., Pettay, Dorothy, Taft, Lisa, Allran, Katherine, Freeman, Sallie B., Karadima, Georgia, Avramopoulos, Dimitris, Torfs, Claudine, Mikkelsen, Margareta, Hassold, Terry J., Sherman, Stephanie L.

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Parental Origin of the Extra Chromosome in Trisomy 21 as Indicated by Analysis of DNA Polymorphisms von Antonarakis, Stylianos E

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Apolipoprotein E allele distribution in parents of Down's syndrome children von Avramopoulos, D., Grigoriadou, M., Petersen, M.B., Mikkelsen, M., Petersen, M.B., Vassilopoulos, D.

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THE MEIOTIC STAGE OF NONDISJUNCTION IN TRISOMY-21 - DETERMINATION BY USING DNA POLYMORPHISMS von ANTONARAKIS, SE, PETERSEN, MB, MCINNIS, MG, ADELSBERGER, PA, SCHINZEL, AA, BINKERT, F, PANGALOS, C, RAOUL, O, SLAUGENHAUPT, SA, HAFEZ, M, COHEN, MM, ROULSON, D, SCHWARTZ, S, MIKKELSEN, M, TRANEBJAERG, L, GREENBERG, F, HOAR, DI, RUDD, NL, WARREN, AC, METAXOTOU, C, BARTSOCAS, C, CHAKRAVARTI, A

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Molecular genetic approach to the characterization of the “Down syndrome region” of chromosome 21 von McCormick, Mary Kay, Schinzel, Albert, Petersen, Michael B., Stetten, Gail, Driscoll, Daniel J., Cantu, Eduardo S., Tranebjaerg, Lisbeth, Mikkelsen, Margareta, Watkins, Paul C., Antonarakis, Stylianos E.

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Analysis of a whole arm translocation between chromosomes 18 and 20 using fluorescence in situ hybridization: detection of a break in the centromeric ?-satellite sequences von T mer, Zeynep, Berg, Anna, Mikkelsen, Margareta

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Analysis of a whole arm translocation between chromosomes 18 and 20 using fluorescence in situ hybridization : detection of a break in the centromeric α-satellite sequences von TÜMER, Z, BERG, A, MIKKELSEN, M

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Uniparental isodisomy due to duplication of chromosome 21 occuring in somatic cells monosomic for chromosome 21 von Petersen, Michael B., Bartsch, Oliver, Adelsberger, Patricia A., Mikkelsen, Margareta, Schwinger, Eberhard, Antonarakis, Stylianos E.

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