Zobrazeno 1 - 10
of 91
pro vyhledávání: '"P. Mollevanger"'
Autor:
F. H. M. Cluitmans, J. W. Wessels, P. Mollevanger, Geoffrey C. Beverstock, Martijn H. Breuning, J. G. Dauwerse
Publikováno v:
Blood. 77:1555-1559
We report a case of acute nonlymphocytic leukemia (ANLL) M5 with the characteristic t(8;16)(p11;p13). The breakpoint in the short arm was regionally localized using nonradioactive in situ hybridization with a series of cosmids of chromosome 16. The r
Autor:
S. Warter, B. Brun, T.A. Donlon, S. Chamberlain, N. Shimizu, S. Minoshima, G.T. O’Neill, P. Mollevanger, T.B. Shows, C. Morris, M. Hauwy, S. Speirs, T.R. Tiersch, J.W. Wessels, P. Devilee, J.C. Winkelmann, P.C. Watkins, D. Nakamura, J.W. Oosterhuis, J. Koch, C. García de la Vega, M. Douglass, Y. Fukushima, J.M. Martínez Zapater, M.G. Byers, N. Heisterkamp, C.J. Cornelisse, R. Fukuyama, A.J. Driesel, C. Clayberger, R.W. Chandler, Q.L. Hao, J. Gosálvez, A.M. Krensky, Y. Shimizu, J. Shaw, P.B. Moens, T. Ashley, V.T.H.B.M. Smit, J. Groffen, N. Tommerup, V. Goyanes, R. Mezzanotte, B.G. Forget, P. Lichter, M.H. Kaufman, S. Ohno, Y. Rumpler, J.R. Testa, R.E. Pearlman, R. Williamson, L.B. Andersen, L.H.J. Looijenga, S. Ohmi-Imajohs, C. López-Fernández, N.L.A. Cacheiro, K. Suzuki, J. Kudoh
Publikováno v:
Cytogenetic and Genome Research. 53:I-IV
Autor:
G C, Beverstock, P, Mollevanger, M, Baaij, J, Lind, L, van Ieperen, M M, Bartelings, K, Teunissen, H, Brandenburg, D, Van Opstal, F, Los
Publikováno v:
Cancer genetics and cytogenetics. 115(1)
The occurrence of nasopharyngeal teratomas (NPT) is an infrequent event and prenatal detection of such tumors is even rarer. We present a case report and review of the literature (N = 78 cases), in which we describe the cytogenetic, DNA, and patholog
Autor:
Vincent T.H.B.M. Smit, J.W. Oosterhuis, C.J. Cornelisse, Leendert H. J. Looijenga, P. Mollevanger, Peter Devilee, J.W. Wessels
Publikováno v:
Cytogenetic and Genome Research. 53:216-218
The isolation and localization of a chromosome 12-specific α satellite DNA sequence, pα12H8, is described. This clone contains a complete copy of the 1.4-kb Hindlll higher-order repeat present within the α satellite array on chromosome 12. The spe
Autor:
S L, van Zelderen-Bhola, J V, Bovée, H W, Wessels, P, Mollevanger, J V, Nijhuis, J D, van Eendenburg, A H, Taminiau, P C, Hogendoorn
Publikováno v:
Cancer genetics and cytogenetics. 105(2)
Chromosome analysis of a chondroblastoma of the right distal femur in a 31-year-old male patient revealed a ring chromosome 4 in approximately one-third of the analyzed cells. The remaining cells had a normal karyotype. These findings were subsequent
Autor:
M. C. Lindeman-Kusse, P. Mollevanger, Dian Donnai, Geoffrey C. Beverstock, I. Stec, Egbert Bakker, G.J.B. van Ommen, Sarina G. Kant, A. van Haeringen
Recently, a deletion of chromosome 4pter was found in three patients with Pitt-Rogers-Danks syndrome. We investigated two of these patients, by means of DNA and FISH studies, together with two additional patients with Pitt-Rogers-Danks syndrome, to d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6137d5db6dfb2adcec1b3b1c311d246d
https://europepmc.org/articles/PMC1050997/
https://europepmc.org/articles/PMC1050997/
Autor:
Christina Lich, E Sleegers, G Schwanitz, G Beverstock, A. M. W. Van Den Ouweland, Bernhard Horsthemke, Gabriele Gillessen-Kaesbach, Anneke Maat-Kievit, P Mollevanger, Karin Buiting
Publikováno v:
Journal of medical genetics. 33(10)
A de novo interstitial deletion of 15q11-q13 is the major cause of Prader-Willi syndrome (PWS) and Angelman syndrome (AS). Here we describe two unrelated PWS patients with a typical deletion, whose fathers have a balanced translocation involving the
Autor:
Leendert H. J. Looijenga, Vincent T.H.B.M. Smit, Jw Oosterhuis, Peter Devilee, J.W. Wessels, P. Mollevanger
Publikováno v:
Genomics. 13(4)
We have investigated the organization and complexity of alpha satellite DNA on chromosomes 10 and 12 by restriction endonuclease mapping, in situ hybridization (ISH), and DNA-sequencing methods. Alpha satellite DNA on both chromosomes displays a basi
Publikováno v:
Clinical genetics. 41(2)
A girl with a 71,XXXXY karyotype is described. Internal and external genitalia were female despite the presence of a Y-chromosome.
Autor:
G.J.B. van Ommen, Kenneth H. Fischbeck, E. J. Meershoek, K.L. Chen, M.S. Driesen, P. Mollevanger, Martin C. Wapenaar, J. G. Dauwerse
Publikováno v:
Genomics. 11(4)
A yeast artificial chromosome (YAC) library has been constructed from a somatic cell hybrid containing a t(1p;19q) chromosome and chromosome 17. After amplification, part of this library was analyzed by high-density colony filter screening with a rep