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British Journal of Haematology|January 17, 2007
Abnormalities of chromosome 1p/q are highly associated with chromosome 13/13q deletions and are an adverse prognostic factor for the outcome of high-dose chemotherapy in patients with multiple myelomaKa Lung Wu, Berna Beverloo, Henk M Lokhorst, et al.
Developmental Medicine and Child Neurology|March 18, 2011
Long-term follow-up of type 1 lissencephaly: survival is related to neuroimaging abnormalitiesMarie-Claire Y de Wit, Jojanneke de Rijk-van Andel, Dicky J Halley, et al.
Molecular Cytogenetics|July 13, 2010
Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomaliesLars T van der Veken, Marianne Mj Dieleman, Hannie Douben, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|August 13, 2009
Implication of long-distance regulation of the HOXA cluster in a patient with postaxial polydactylyElisabeth M Lodder, Bert H Eussen, Daniëlla A C M van Hassel, et al.
European Journal of Human Genetics : EJHG|June 17, 2010
5q11.2 deletion in a patient with tracheal agenesisElisabeth M de Jong, Hannie Douben, Bert H Eussen, et al.
American Journal of Medical Genetics. Part A|August 5, 2010
Phenotypic spectrum of 20 novel patients with molecularly defined supernumerary marker chromosomes 15 and a review of the literatureTjitske Kleefstra, Nicole de Leeuw, Roy Wolf, et al.
European Journal of Human Genetics : EJHG|January 9, 2014
Structural and numerical changes of chromosome X in patients with esophageal atresiaErwin Brosens, Elisabeth M de Jong, Tahsin Stefan Barakat, et al.
American Journal of Medical Genetics. Part A|May 19, 2009
Interstitial 11q deletion derived from a maternal ins(4;11)(p14;q24.2q25): a patient report and reviewLaura J C M Van Zutven, Yolande van Bever, Carolien C M Van Nieuwland, et al.
The Journal of Pathology|October 11, 2002
Numerical aberrations of chromosome 1 in cervical intraepithelial neoplasia are strongly associated with infection with high-risk human papillomavirus typesJohan Bulten, Willem J G Melchers, Maria M Kooy-Smits, et al.
American Journal of Medical Genetics. Part A|January 11, 2013
Complex craniosynostosis is associated with the 2p15p16.1 microdeletion syndromeJoyce M G Florisson, Irene M J Mathijssen, Belinda Dumee, et al.
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