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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Prevalence and Phenotype Consequence of FRAXA and FRAXE Alleles in a Large, Ethnically Diverse, Special Education–Needs Population von Crawford, Dana C., Meadows, Kellen L., Newman, James L., Taft, Lisa F., Pettay, Dorothy L., Gold, Laura B., Hersey, S. Jane, Hinkle, Elizabeth F., Stanfield, Mary L., Holmgreen, Patricia, Yeargin-Allsopp, Marshalyn, Boyle, Coleen, Sherman, Stephanie L.

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Reconstructing hominid Y evolution : X-homologous block, created by X-Y transposition, was disrupted by Yp inversion through line-line recombination von SCHWARTZ, A, CHAN, D. C, BROWN, L. G, ALAGAPPAN, R, PETTAY, D, DISTECHE, C, MCGILLIVRAY, B, DE LA CHAPELLE, A, PAGE, D. C

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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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Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of the chromosomal error : A population-based study von YOON, P. W, FREEMAN, S. B, SHERMAN, S. L, TAFT, L. F, YUANCHAO GU, PETTAY, D, FLANDERS, W. D, KHOURY, M. J, HASSOLD, T. J

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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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XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region von HASSOLD, T. J, SHERMAN, S. L, PETTAY, D, PAGE, D. C, JACOBS, P. A

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MOLECULAR STUDIES OF PARENTAL ORIGIN AND MOSAICISM IN 45,X-CONCEPTUSES von HASSOLD, T, PETTAY, D, ROBINSON, A, UCHIDA

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Cytogenetic and molecular study of four couples with multiple trisomy 21 pregnancies von James, R S, Ellis, K, Pettay, D, Jacobs, P A

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Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy von HASSOLD, T, PETTAY, D, MAY, K, ROBINSON, A

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Risk factors for trisomy 21: Maternal cigarette smoking and oral contraceptive use in a spopulation-based case-control study von Yang, Quanhe, Sherman, Stephanie L., Hassold, Terry J., Allran, Katherine, Taft, Lisa, Pettay, Dorothy, Khoury, Muin J., Erickson, J. David, Freeman, Sallie B.

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Analysis of nucleolar organizing regions in parents of trisomic spontaneous abortions von HASSOLD, T, JACOBS, P. A, PETTAY, D

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The effect of caffeine on fragile X expression von ABRUZZO, M. A, PETTAY, D, MAYER, M, JACOBS, P. A

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Cytogenetic studies of couples with repeated spontaneous abortions of known karyotype von Hassold, Terry, Jacobs, Patricia A., Pettay, Dorothy, Rao, D. C.

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Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population von Meadows, Kellen L., Pettay, Dorothy, Newman, James, Hersey, Jane, Ashley, Allison E., Sherman, Stephanie L.

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Asplenia syndrome in a child with a balanced reciprocal translocation of chromosomes 11 and 20 [46,XX,t(11;20)(q13.1;q13.13)] von Freeman, Sallie B., Muralidharan, Kasinathan, Pettay, Dorothy, Blackston, R. Dwain, May, Kristin M.

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