In Vitro Fertilization with Preimplantation Genetic Screening von Mastenbroek, Sebastiaan, Twisk, Moniek, van Echten-Arends, Jannie, Sikkema-Raddatz, Birgit, Korevaar, Johanna C, Verhoeve, Harold R, Vogel, Niels E.A, Arts, Eus G.J.M, de Vries, Jan W.A, Bossuyt, Patrick M, Buys, Charles H.C.M, Heineman, Maas Jan, Repping, Sjoerd, van der Veen, Fulco

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Molecular and Clinical Characteristics of MSH6 Variants: An Analysis of 25 Index Carriers of a Germline Variant von Berends, Maran J.W., Wu, Ying, Sijmons, Rolf H., Mensink, Rob G.J., van der Sluis, Tineke, Hordijk-Hos, Jannet M., de Vries, Elisabeth G.E., Hollema, Harry, Karrenbeld, Arend, Buys, Charles H. C.M., van der Zee, Ate G.J., Hofstra, Robert M.W., Kleibeuker, Jan H.

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MUTYH and the mismatch repair system : partners in crime? von NIESSEN, Renée C, SIJMONS, Rolf H, DE BOCK, Geertruida H, BUYS, Charles H. C. M, KLEIBEUKER, Jan H, HOFSTRA, Robert M. W, OU, J, OLTHOF, Sandra G. M, OSINGA, Jan, LIGTENBERG, Marjolijn J, HOGERVORST, Frans B. L, WEISS, Marjan M, TOPS, Carli M. J, HES, Frederik J

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Identifying Candidate Hirschsprung Disease–Associated RET Variants von Burzynski, Grzegorz M., Nolte, Ilja M., Bronda, Agnes, Bos, Krista K., Osinga, Jan, Plaza Menacho, Ivan, Twigt, Bas, Maas, Saskia, Brooks, Alice S., Joke Verheij, B.G.M., Charles Buys, H.C.M., Robert Hofstra, M.W.

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FISH and array‐CGH analysis of a complex chromosome 3 aberration suggests that loss of CNTN4 and CRBN contributes to mental retardation in 3pter deletions von Dijkhuizen, Trijnie, van Essen, Ton, van der Vlies, Pieter, Verheij, Joke B.G.M., Sikkema‐Raddatz, Birgit, van der Veen, Anneke Y., Gerssen‐Schoorl, Klasien B.J., Buys, Charles H.C.M., Kok, Klaas

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First-trimester use of paroxetine and congenital heart defects: A population-based case-control study von Bakker, Marian K., Kerstjens-Frederikse, Wilhelmina S., Buys, Charles H. C. M., de Walle, Hermien E. K., de Jong-van den Berg, Lolkje T. W.

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Inheritance mode of multiple sclerosis: the effect of HLA class II alleles is stronger than additive von BOON, Maartje, NOLTE, Ilja M, DE KEYSER, Jacques, BUYS, Charles H. C. M, TE MEERMAN, Gerard J

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Determination of TP53 Mutation Is More Relevant Than Microsatellite Instability Status for the Prediction of Disease-Free Survival in Adjuvant-Treated Stage III Colon Cancer Patien... von WESTRA, Jantine L, SCHAAPVELD, Michael, PLUKKER, John T. M, HOLLEMA, Harry, DE BOER, Jelle P, KRAAK, Marian M. J, DE JONG, Debora, TER ELST, Arja, MULDER, Nanno H, BUYS, Charles H. C. M, HOFSTRA, Robert M. W

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RET-familial medullary thyroid carcinoma mutants Y791F and S891A activate a Src/JAK/STAT3 pathway, independent of glial cell line-derived neurotrophic factor von MENACHO, Ivan Plaza, KOSTER, Roelof, EGGEN, Bart J. L, HOFSTRA, Robert M. W, VAN DER SLOOT, Almer M, QUAX, Wim J, OSINGA, Jan, VAN DER SLUIS, Tineke, HOLLEMA, Harry, BURZYNSKI, Grzegorz M, GIMM, Oliver, BUYS, Charles H. C. M

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Quality aspects of prenatal cytogenetic diagnosis: determining the effect of various factors involved in handling amniotic fluid and chorionic villus material for cytogenetic diagn... von Sikkema-Raddatz, Birgit, Suijkerbuijk, Ron, Bouman, Katelijne, de Jong, Bauke, Buys, Charles H.C.M., te Meerman, Gerard J.

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Toward New Strategies to Select Young Endometrial Cancer Patients for Mismatch Repair Gene Mutation Analysis von Berends, Maran J W, Wu, Ying, Sijmons, Rolf H, van der Sluis, Tineke, Ek, Wietske Boersmavan, Ligtenberg, Marjolijn J L, Arts, Neeltje J W, ten Hoor, Klaske A, Kleibeuker, Jan H, de Vries, Elisabeth G E, Mourits, Marian J E, Hollema, Harry, Buys, Charles H C M, Hofstra, Robert M W, van der Zee, Ate G J

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A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma von Hofstra, Robert M. W, Landsvater, Rudy M, Ceccherini, Isabella, Stulp, Rein P, Stelwagen, Tineke, Luo, Yin, Pasini, Barbara, Hoppener, Jo W. M, van Amstel, Hans Kristian Ploos, Romeo, Giovanni, Lips, Cornells J. M, Buys, Charles H. C. M

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A Human Model for Multigenic Inheritance: Phenotypic Expression in Hirschsprung Disease Requires Both the RET Gene and a New 9q31 Locus von Bolk, Stacey, Pelet, Anna, Robert M. W. Hofstra, Angrist, Misha, Salomon, Remi, Croaker, David, Charles H. C. M. Buys, Lyonnet, Stanislas, Chakravarti, Aravinda

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An absolute procedure to test the growth potential of medium and the influence of decreased oxygen tension in primary amniotic fluid cell cultures von Sikkema-Raddatz, Birgit, Suijkerbuijk, Ron, van der Vlag, Jakob, Stoepker, Marian, Buys, Charles H. C. M., te Meerman, Gerard J.

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Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancer von Kok, Klaas, Osinga, Jan, Carritt, Ben, Davis, Mary B, van der Hout, Annemarie H, van der Veen, Anneke Y, Landsvater, Rudy M, de Leij, Lou F. M. H, Berendsen, Henk H, Postmus, Pieter E, Poppema, Sibrand, Buys, Charles H. C. M

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Analysis of a new homozygous deletion in the tumor suppressor region at 3p12.3 reveals two novel intronic noncoding RNA genes von Angeloni, Debora, ter Elst, Arja, Wei, Ming Hui, van der Veen, Anneke Y., Braga, Eleonora A., Klimov, Eugene A., Timmer, Tineke, Korobeinikova, Luba, Lerman, Michael I., Buys, Charles H.C.M.

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Partial Revertant Mosaicism of Keratin 14 in a Patient with Recessive Epidermolysis Bullosa Simplex von SCHUILENGA-HUT, Petra H. L, SCHEFFER, Hans, PAS, Hendri H, NIJENHUIS, Miranda, BUYS, Charles H. C. M, JONKMAN, Marcel F

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Localizing a putative mutation as the major contributor to the development of sporadic Hirschsprung disease to the RET genomic sequence between the promoter region and exon 2 von Burzynski, Grzegorz M, Nolte, Ilja M, Osinga, Jan, Ceccherini, Isabella, Twigt, Bas, Maas, Saskia, Brooks, Alice, Verheij, Joke, Menacho, Ivan Plaza, Buys, Charles HCM, Hofstra, Robert MW

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Mutation analysis of the entire keratin 5 and 14 genes in patients with epidermolysis bullosa simplex and identification of novel mutations von Schuilenga-Hut, Petra H.L., Vlies, Pieter v.d., Jonkman, Marcel F., Waanders, Esmé, Buys, Charles H.C.M., Scheffer, Hans

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Functional analysis of lung tumor suppressor activity at 3p21.3 von ter Elst, Arja, Hiemstra, Bea E., van der Vlies, Pieter, Kamminga, Wytske, van der Veen, Anneke Y., Davelaar, Inge, Terpstra, Peter, te Meerman, Gerard J., Gerbens, Frans, Kok, Klaas, Buys, Charles H. C. M.

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