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

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NO EVIDENCE FOR A PATERNAL INTERCHROMOSOMAL EFFECT FROM ANALYSIS OF THE ORIGIN OF NONDISJUNCTION IN DOWN-SYNDROME PATIENTS WITH CONCOMITANT FAMILIAL CHROMOSOME REARRANGEMENTS von SCHINZEL, AA, ADELSBERGER, PA, BINKERT, F, BASARAN, S, ANTONARAKIS, SE

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Down syndrome due to de novo Robertsonian translocation t(14q;21q) : DNA polymorphism analysis suggests that the origin of the extra 21q is maternal von PETERSEN, M. B, ADELSBERGER, P. A, SCHINZEL, A. A, BINKERT, F, HINKEL, G. K, ANTONARAKIS, S. E

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A 48,XXY,+21 down syndrome patient with additional paternal X and maternal 21 von LORDA-SANCHEZ, I, PETERSEN, M. B, BINKERT, F, MAECHLER, M, SCHMID, W, ADELSBERGER, P. A, ANTONARAKIS, S. E, SCHINZEL, A

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Analysis of DNA polymorphisms suggests that most de novo dup(21q) chromosomes in patients with Down syndrome are isochromosomes and not translocations von Antonarakis, Stylianos E, Adelsberger, Patricia A, Petersen, Michael B, Binkert, Franz, Schinzel, Albert A

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Down syndrome due to de novo Robertsonian translocation t(14q;21q): DNA polymorphism analysis suggests that the origin of the extra 21q is maternal von Petersen, Michael B, Adelsberger, Patricia A, Schinzel, Albert A, Binkert, Franz, Hinkel, Georg K, Antonarakis, Stylianos E

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A 48,XXY,+21 Down syndrome patient with additional paternal X and maternal 21 von Lorda-Sanchez, Isabel, Petersen, Michael B, Binkert, Franz, Maechler, Marco, Schmid, Werner, Adelsberger, Patricia A, Antonarakis, Stylianos E, Schinzel, Albert

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DNA polymorphism analysis in families with recurrence of free trisomy 21 von Pangalos, Constantinos G, Talbot Jr., Conover C, Lewis, John G, Adelsberger, Patricia A, Petersen, Michael B, Serre, Jean-Louis, Rethoré, Marie-Odile, de Blois, Marie-Christine, Parent, Philipe, Schinzel, Albert A, Binkert, Franz, Boue, Joelle, Corbin, Elisabeth, Croquette, M F, Gilgenkrantz, Simone, de Grouchy, Jean, Bertheas, M F, Prieur, Marguerite, Raoul, Odile, Serville, Framcoise, Siffroi, J P, Thepot, Francois, Lejeune, Jerome, Antonarakis, Stylianos E

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The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms von Antonarakis, Stylianos E, Petersen, Michael B, McInnis, Melvin G, Adelsberger, Patricia A, Schinzel, Albert A, Binkert, Franz, Pangalos, Constantine, Raoul, Odile, Slaugenhaupt, Susan A, Hafez, Mohamed, Cohen, Maimon M, Roulson, Diane, Hoar, David I, Rudd, Noreen L, Warren, Andrew C, Metaxotou, Caterina, Bartsocas, Christos, Chakravarti, Aravinda

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