An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito by Eussen, Bert H J, Bartalini, Gabriella, Bakker, Lida, Balestri, Paolo, Di Lucca, Carmela, Van Hemel, Jan O, Dauwerse, Hans, van den Ouweland, Ans M W, Ris-Stalpers, Carrie, Verhoef, Senno, Halley, Dicky J J, Fois, Alberto

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Molecular Cytogenetic Analysis of Eight Inversion Duplications of Human Chromosome 13q That Each Contain a Neocentromere by Warburton, Peter E., Dolled, Marisa, Mahmood, Radma, Alonso, Alicia, Li, Shulan, Naritomi, Kenji, Tohma, Takaya, Nagai, Toshiro, Hasegawa, Tomonobu, Ohashi, Hirofumi, Govaerts, Lutgarde C.P., Eussen, Bert H.J., Van Hemel, Jan O., Lozzio, Carmen, Schwartz, Stuart, Dowhanick-Morrissette, Jennifer J., Spinner, Nancy B., Rivera, Horacio, Crolla, John A., Yu, Chih-yu, Warburton, Dorothy

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Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family by de Vries, B B, Jansen, C C, Duits, A A, Verheij, C, Willemsen, R, van Hemel, J O, van den Ouweland, A M, Niermeijer, M F, Oostra, B A, Halley, D J

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Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndrome by Wouters, Cokkie H., Meijers-Heijboer, Hanne J., Eussen, Bert J.F.M.M., van der Heide, Annette A., van Luijk, Rob B., van Drunen, Ellen, Beverloo, Berna B., Visscher, Frank, Van Hemel, Jan O.

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CHARGE association-related ocular pathology in a newborn with partial trisomy 19q and partial monosomy 21q, from a maternal translocation (19;21) (q13.1;q22.3) by De Krijger, R R, Mooy, C M, Van Hemel, J O, Sulkers, E J, Kros, J M, Bartelings, M M, Govaerts, L C

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DNA diagnosis of Prader-Willi and Angelman syndromes with the probe PW71 (D15S63) by VAN DEN OUWELAND, A. M. W, VAN DER EST, M. N, WESBY-VAN SWAAY, E, TIJMENSEN, T. S. L. N, LOS, F. J, VAN HEMEL, J. O, HENNEKAM, R. C. M, MEIJERS-HEIJBOER, H. J, NIERMEIJER, M. F, HALLEY, D. J. J

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De novo deletion (2) (p11.2p13): clinical, cytogenetic, and immunological data by Los, F J, Van Hemel, J O, Jacobs, H J, Drop, S L, van Dongen, J J

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Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14) by de Vries, Bert B.A., Eussen, Bert H.J., van Diggelen, Otto P., van der Heide, Annet, Deelen, Wouter H., Govaerts, Lutgarde C.P., Lindhout, Dick, Wouters, Cokkie H., Van Hemel, Jan O.

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Partial trisomy 10q: a recognizable syndrome by 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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Towards in vivo characterization of thyroid nodules suspicious for malignancy using multispectral optoacoustic tomography by Noltes, Milou E., Bader, Maximilian, Metman, Madelon J. H., Vonk, Jasper, Steinkamp, Pieter J., Kukačka, Jan, Westerlaan, Henriette E., Dierckx, Rudi A. J. O., van Hemel, Bettien M., Brouwers, Adrienne H., van Dam, Gooitzen M., Jüstel, Dominik, Ntziachristos, Vasilis, Kruijff, Schelto

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Pressure–volume loop analysis during implantation of biventricular pacemaker/cardiac resynchronization therapy device to optimize right and left ventricular pacing sites by Delnoy, Peter Paul H.M., Ottervanger, Jan Paul, Luttikhuis, Henk Oude, Vos, Dick H.S., Elvan, Arif, Ramdat Misier, Anand R., Beukema, Willem P., Steendijk, Paul, van Hemel, Norbert M.

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Two cases of Robertsonian translocations in oligozoospermic males and their consequences for pregnancies induced by intracytoplasmic sperm injection by Veld, P A, Weber, R F, Los, F J, den Hollander, N, Dhont, M, Pieters, M H, Van Hemel, J O

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