Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience von Tuerlings, JHAM, de France, HF, Hamers, A, Hordijk, R, Van Hemel, JO, Hansson, K, Hoovers, JMN, Madan, K, Van Der Blij-Philipsen, M, Gerssen-Schoorl, KBJ, Kremer, JAM, Smeets, DFCM

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Intracytoplasmic sperm injection (ICSI) and chromosomally abnormal spermatozoa von In't Veld, P A, Broekmans, F J, de France, H F, Pearson, P L, Pieters, M H, van Kooij, R J

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Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience von Tuerlings, J H, de France, H F, Hamers, A, Hordijk, R, Van Hemel, J O, Hansson, K, Hoovers, J M, Madan, K, Van der Blij-Philipsen, M, Gerssen-Schoorl, K B, Kremer, J A, Smeets, D F

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ARE DOWN SYNDROME FETUSES DETECTED THROUGH MATERNAL SERUM SCREENING SIMILAR TO THOSE REMAINING UNDETECTED? von CHRISTIAENS, G. C. M. L., HAGENAARS, A. M., AKKERMAN, C., DE FRANCE, H. F

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A third case of de novo partial trisomy 4p von Oorthuys, J W, Gerssen-Schoorl, K B, de Pater, J M, de France, H F

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Interstitial deletion of the long arm of chromosome 11 von Klep-de Pater, J M, de France, H F, Bijlsma, J B

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Two cases with different deletions of the long arm of chromosome 7 von Klep-de Pater, J M, Bijlsma, J B, Bleeker-Wagemakers, E M, de France, H F, de Vries-Ekkers, C M

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Cytogenetic investigations in volunteers ingesting inorganic lead von Bijlsma, J B, de France, H F

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On the use of distribution-functions to describe and classify chromosome density-profiles von van den Berg, H.T.C.M., Habbema, J.D.F., de France, H.F., Bakker, H.K., de Vries, G.A.

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18q− and 18q+ mosaicism in a mentally retarded boy von Ausems, Margreet G. E. M., Bhola, Shama L., Post-Blok, Cornelie A., Hennekam, Raoul C. M., de France, Henny F.

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The Dutch uniform multicenter registration system for genetic disorders and malformation syndromes von Zwamborn-Hanssen, A. Monic N., Bijlsma, Jan B., Hennekam, Eric F. A. M., Lindhout, Dick, Beemer, Frits A., Bakker, Egbert, Kleijer, Wim J., de France, Henny F., de Die-Smulders, Christine E. M., Duran, Martinus, van Gennip, Albert H., van Mens, J. Theo, Pearson, Peter L., Mantel, Gerrit, Verhage, Rob E., Geraedts, Joep P. M.

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Automated selection of metaphase cells by quality von van den Berg, H. T. C. M., de France, H. F., Habbema, J. D. F., Raatgever, J. W.

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Congenital glaucoma in a child with partial lq duplication and 9p deletion von Verbraak, Frank D., Pogány, Katalin, Pilon, Jan-Willem, Mooy, C. m., De France, H. F., Hennekam, Raoul C.m., Bleeker-Wagemakers, E. M.

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Partial trisomy 6p due to familial translocation t(6;20)(p21;p13). A new syndrome? von Breuning, M H, Bijlsma, J B, de France, H F

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Double translocation t(7;12),t(2;6) heterozygosity in one family. A contribution to the trisomy 12p syndrome von Bijlsma, J B, de France, H F, Bleeker-Wagemakers, L M, Dijkstra, P F

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Partial trisomy 10q: a recognizable syndrome von Klep-de Pater, J M, Bijlsma, J B, de France, H F, Leschot, N J, Duijndam-van den Berge, M, van Hemel, J O

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Cardiovascular and Renal Outcomes with Empagliflozin in Heart Failure von Packer, Milton, Anker, Stefan D, Butler, Javed, Filippatos, Gerasimos, Pocock, Stuart J, Carson, Peter, Januzzi, James, Verma, Subodh, Tsutsui, Hiroyuki, Brueckmann, Martina, Jamal, Waheed, Kimura, Karen, Schnee, Janet, Zeller, Cordula, Cotton, Daniel, Bocchi, Edimar, Böhm, Michael, Choi, Dong-Ju, Chopra, Vijay, Chuquiure, Eduardo, Giannetti, Nadia, Janssens, Stefan, Zhang, Jian, Gonzalez Juanatey, Jose R, Kaul, Sanjay, Brunner-La Rocca, Hans-Peter, Merkely, Bela, Nicholls, Stephen J, Perrone, Sergio, Pina, Ileana, Ponikowski, Piotr, Sattar, Naveed, Senni, Michele, Seronde, Marie-France, Spinar, Jindrich, Squire, Iain, Taddei, Stefano, Wanner, Christoph, Zannad, Faiez

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Congenital glaucoma in a child with partial 1q duplication and 9p deletion von Verbraak, F D, Pogány, K, Pilon, J W, Mooy, C M, de France, H F, Hennekam, R C, Bleeker-Wagemakers, E M

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A third case of de novo partial trisomy 4 p von OORTHUYS, J. W. E, GERSSEN-SCHOORL, K. B. J, DE PATER, J. M, DE FRANCE, H. F

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Intestitial deletion of the long arm of chromosome 11 von KLEP-DE PATER, J. M, DE FRANCE, H. F, BIJLSMA, J. B

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