Hakutulokset - McFadden, D E

Phenotype of triploid embryos Tekijä McFadden, D E, Robinson, W P

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The Origin of Abnormalities in Recurrent Aneuploidy/Polyploidy Tekijä Robinson, W. P., McFadden, D. E., Stephenson, M. D.

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Renal tubular dysgenesis with calvarial hypoplasia: report of two additional cases and review. Tekijä McFadden, D E, Pantzar, J T, Van Allen, M I, Langlois, S

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Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variants Tekijä Filges, I., Manokhina, I., Peñaherrera, M.S., McFadden, D.E., Louie, K., Nosova, E., Friedman, J.M., Robinson, W.P.

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Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome. Tekijä Drumheller, T, McGillivray, B C, Behrner, D, MacLeod, P, McFadden, D E, Roberson, J, Venditti, C, Chorney, K, Chorney, M, Smith, D I

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Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia Tekijä Kaiser‐Rogers, K A, McFadden, D E, Livasy, C A, Dansereau, J, Jiang, R, Knops, J F, Lefebvre, L, Rao, K W, Robinson, W P

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