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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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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Mutational analysis of the FMR1 gene in 118 mentally retarded males suspected of fragile X syndrome : absence of prevalent mutations von GRØNSKOV, K, HALLBERG, A, BRØNDUM-NIELSEN, K

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Hydatidiform mole: a chromosomal search for a recessive mutation von Vejerslev, Lars O., Hallberg, Anni, Tommerup, Niels

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Maternal and paternal origin of extra chromosome in trisomy 21 von Mikkelsen, M, Hallberg, A, Poulsen, H

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Hydatidiform moles: Methods for culture and cytogenetic analyses von Vejerslev, Lars O., Tommerup, Niels, Hallberg, Anni

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