Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II
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
Published in Nature genetics (01.12.1996)
Published in Nature genetics (01.12.1996)
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Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination
Sherman, S L, Petersen, M B, Freeman, S B, Hersey, J, Pettay, D, Taft, L, Frantzen, M, Mikkelsen, M, Hassold, T J
Published in Human molecular genetics (01.09.1994)
Published in Human molecular genetics (01.09.1994)
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Characterization of Susceptible Chiasma Configurations that Increase the Risk for Maternal Nondisjunction of Chromosome 21
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.
Published in Human molecular genetics (01.09.1997)
Published in Human molecular genetics (01.09.1997)
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Prevalence and Phenotype Consequence of FRAXA and FRAXE Alleles in a Large, Ethnically Diverse, Special Education–Needs Population
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.
Published in American journal of human genetics (01.02.1999)
Published in American journal of human genetics (01.02.1999)
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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
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
Published in American journal of human genetics (01.03.1996)
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Published in American journal of human genetics (01.03.1996)
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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
SCHWARTZ, A, CHAN, D. C, BROWN, L. G, ALAGAPPAN, R, PETTAY, D, DISTECHE, C, MCGILLIVRAY, B, DE LA CHAPELLE, A, PAGE, D. C
Published in Human molecular genetics (1998)
Published in Human molecular genetics (1998)
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Elucidating the Mechanisms of Paternal Non-Disjunction of Chromosome 21 in Humans
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.
Published in Human molecular genetics (01.08.1998)
Published in Human molecular genetics (01.08.1998)
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Cytogenetic and molecular study of four couples with multiple trisomy 21 pregnancies
James, R S, Ellis, K, Pettay, D, Jacobs, P A
Published in European journal of human genetics : EJHG (01.05.1998)
Published in European journal of human genetics : EJHG (01.05.1998)
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Risk factors for trisomy 21: Maternal cigarette smoking and oral contraceptive use in a spopulation-based case-control study
Yang, Quanhe, Sherman, Stephanie L., Hassold, Terry J., Allran, Katherine, Taft, Lisa, Pettay, Dorothy, Khoury, Muin J., Erickson, J. David, Freeman, Sallie B.
Published in Genetics in medicine (01.03.1999)
Published in Genetics in medicine (01.03.1999)
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