BRCA1 mutation carriers have a lower number of mature oocytes after ovarian stimulation for IVF/PGD von Derks-Smeets, I. A. P., van Tilborg, T. C., van Montfoort, A., Smits, L., Torrance, H. L., Meijer-Hoogeveen, M., Broekmans, F., Dreesen, J. C. F. M., Paulussen, A. D. C., Tjan-Heijnen, V. C. G., Homminga, I., van den Berg, M. M. J., Ausems, M. G. E. M., de Rycke, M., de Die-Smulders, C. E. M., Verpoest, W., van Golde, R.

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Preimplantation genetic testing for more than one genetic condition: clinical and ethical considerations and dilemmas von van der Schoot, V, Dondorp, W, Dreesen, J C F M, Coonen, E, Paulussen, A D C, de Wert, G, de Die-Smulders, C E M

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Multiplex PCR of polymorphic markers flanking the CFTR gene; a general approach for preimplantation genetic diagnosis of cystic fibrosis von Dreesen, J.C.F.M., Jacobs, L.J.A.M., Bras, M., Herbergs, J., Dumoulin, J.C.M., Geraedts, J.P.M., Evers, J.L.H., Smeets, H.J.M.

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Preimplantation genetic diagnosis of spinal muscular atrophy von DREESEN, J. C. F. M, BRAS, M, DE DIE-SMULDERS, C, DUMOULIN, J. C. M, COBBEN, J. M, EVERS, J. L. H, SMEETS, H. J. M, GERAEDTS, J. P. M

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Molecular Cloning and Restriction Endonuclease Mapping of the Rat Cytomegalovirus Genome von Meijer, Henk, Dreesen, Jos C. F. M, van Boven, Cees P. A

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DXS539, a polymorphic DNA marker proximal of the fragile-X gene von DREESEN, J. C. F. M, VAN DEN HURK, J. A. J. M, SMITS, A. P. T, VAN DEN OUWELAND, A. M. W, MARKSLAG, P. W. B, VAN OOST, B. A

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Allelic dropout caused by allele-specific amplification failure in single-cell PCR of the cystic fibrosis ΔF508 deletion von DREESEN, J. C. F. M, BRAS, M, COONEN, E, DUMOULIN, J. C. M, EVERS, J. L. H, GERAEDTS, J. P. M

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RS46(DXS548) genotyping of reproductive cells : approaching preimplantation testing of the fragile-X syndrome von DREESEN, J. C. F. M, GERAEDTS, J. P. M, DUMOULIN, J.C . M, EVERS, J. L. H, PIETERS, M. H. E. C

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First trimester prenatal diagnosis of haemophilia A: Two years' experience von Bröcker-Vriends, A. H. J. T., Briët, E., Kanhai, H. H. H., Bakker, E., Dreesen, J. C. F. M., Leschot, N. J., van de Kamp, J. J. P., Pearson, P. L.

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The fragile X syndrome: no evidence for any recent mutations von Smits, A P, Dreesen, J C, Post, J G, Smeets, D F, de Die-Smulders, C, Spaans-van der Bijl, T, Govaerts, L C, Warren, S T, Oostra, B A, van Oost, B A

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Clinical application of FISH for sex determination of embryos in preimplantation diagnosis of X-linked diseases von COONEN, E, DUMOULIN, J. C. M, DREESEN, J. C. F. M, BRAS, M, EVERS, J. L. H, GERAEDTS, J. P. M

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Somatic origin of inherited haemophilia A von BRÖCKER-VRIENDS, A. H. J. T, BRIËT, E, DREESEN, J. C. F. M, BAKKER, B, REITSMA, P, PANNEKOEK, H, VAN DE KAMP, J. J. P, PEARSON, P. L

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Session 42: Preimplantation Genetic Diagnosis von Uum van, C. M. J., Stevens, S. J. C., Dreesen, J. C. F. M., Drusedau, M., Smeets, H. J. M., Hollander-Crombach, H. T. M., Geraedts, J. P. M., Engelen, J. J. M., Coonen, E., Ling, J., Long, X., Liu, J., Zhuang, G., Cao, B., Xu, K., Mir, P., Rodrigo, L., Cervero, A., Mercader, A., Delgado, A., Buendia, P., Pellicer, A., Rubio, C., Martin, J., Garcia-Quevedo, L., Blanco, J., Sarrate, Z., Bassas, L., Vidal, F., Labarta, E., Bosch, E., Alama, P., Remohi, J.

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Multiplex polymerase chain reaction for sex determination of single mouse blastomeres von DREESEN, J. C. F. M, DUMOULIN, J. C. M, EVERS, J. L. H, GERAEDTS, J. P. M, PIETERS, M. H. E. C

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Mutations in the vasopressin type 2 receptor gene ( AVPR2 ) associated with nephrogenic diabetes insipidus von van den Ouweland, Ans M.W, Dreesen, Jos C.F.M, Verdijk, Marian, Knoers, Nine V.A.M, Monnens, Leo A.H, Rocchi, Mariano, van Oost, Bernard A

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Two polymorphisms at the DXS539 locus von VAN DEN HURK, J. A. J. M, DREESEN, J. C. F. M, VAN DEN BERG, H, VAN BENNEKOM, C. A, VAN DEN OUWELAND, A. M. W, VAN OOST, B. A

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Preimplantation genetic diagnosis of spinocerebellar ataxia 3 by (CAG)(n) repeat detection von Drüsedau, M, Dreesen, J C F M, De Die-Smulders, C, Hardy, K, Bras, M, Dumoulin, J C M, Evers, J L H, Smeets, H J M, Geraedts, J P M, Herbergs, J

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Preimplantation genetic diagnosis of spinocerebellar ataxia 3 by (CAG)n repeat detection von Drüsedau, M., Dreesen, J.C.F.M., de Die‐Smulders, C., Hardy, K., Bras, M., Dumoulin, J.C.M., Evers, J.L.H., Smeets, H.J.M., Geraedts, J.P.M., Herbergs, J.

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Multipoint linkage analysis of DXS369 and DXS304 in fragile X families von van Oost, B. A., Smits, A., Dreesen, J. C. F. M., Smeets, D., Perdon, L., van Bennekom, C. A., Dahl, N., Bakker, E., Oostra, B. A.

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Les meules du Néolithique à l’époque médiévale : technique, culture, diffusion von Alix, Stéphane, Alonso, Natàlia, Anderson, Timothy, Asselin, Guillaume, Aubry, Laurent, Balmelle, Agnès, Barbin, Vincent, Béfort, Jean-Claude, Boyer, François, Brisotto, Vérane, Brkojewitsch, Gael, Brun, Jean-Pierre, Buchsenschutz, Olivier, Carbillet, Aurélie, Chaigneau, Chloe, Cherfa, Kamila, Cnudde, Veerle, Cousseran-Néré, Sylvie, De Clerq, Wim, De Kock, Tim, Donnart, Klet, Dreesen, Roland, Duda, Tristan, Etchart-Salas, Mikel, Font, Caroline, Frankel, Rafaël, Fronteau, Gilles, Frouin, Milena, Galland, Sophie, Garcia, Christian, Georges, Vincent, Gisclon, Jean-Luc, Goemaere, Eric, Hamon, Caroline, Hartoch, Else, Hénon, Philippe, Holderbach, Jean-Marie, Jaccottey, Luc, Jodry, Florent, Koehler, Alain, Larousse, Nicolas Minvielle, Lepareux-Couturier, Stéphanie, Le Quellec, Vincent, Li, Guoqiang, Marquié, Sandrine, Maujean, Johann, Milleville, Annabelle, Minvielle-Larousse, Nicolas, Moiret, François, Monchablon, Cécile, Picavet, Paul, Pruneyrolles, Lucie, Reniere, Sibrecht, Robert, Bruno, Robin, Boris, Rollet, Philippe, Saurel, Marion

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