Genomic imprinting : concept and clinical consequencesMANNENS, M; ALDERS, M.Annals of medicine (Helsinki). 1999, Vol 31, Num 1, pp 4-11, issn 0785-3890Article

The use of genotype-phenotype correlations in mutation analysis for the long QT syndromeVAN LANGEN, I. M; BIRNIE, E; ALDERS, M et al.Journal of medical genetics. 2003, Vol 40, Num 2, pp 141-145, issn 0022-2593, 5 p.Article

Genomic organization and chromosomal localization of a member of the MAP kinase phosphatase gene family to human chromosome 11p15.5 and a pseudogene to 10q11.2NESBIT, M. A; HODGES, M. D; LITTLE, P. F. R et al.Genomics (San Diego, Calif.). 1997, Vol 42, Num 2, pp 284-294, issn 0888-7543Article

Phenotypic discordance upon paternal or maternal transmission of duplications of the 11p15 imprinted regionsBLIEK, J; SNIJDER, S; MAAS, S. M et al.European journal of medical genetics. 2009, Vol 52, Num 6, pp 404-408, issn 1769-7212, 5 p.Article

Two cases of severe neonatal hypertrophic cardiomyopathy caused by compound heterozygous mutations in the MYBPC3 geneLEKANNE DEPREZ, R. H; MUURLING-VLIETMAN, J. J; HRUDA, J et al.Journal of medical genetics. 2006, Vol 43, Num 10, pp 829-832, issn 0022-2593, 4 p.Article

Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndromeALDERS, M; RYAN, A; HODGES, M et al.American journal of human genetics. 2000, Vol 66, Num 5, pp 1473-1484, issn 0002-9297Conference Paper

Report of fifth international Workshop on Human Chromosome 11 Mapping 1996SHOWS, T. B; ALDERS, M; DEVILEE, P et al.Cytogenetics and cell genetics. 1996, Vol 74, Num 1-2, pp 1-56, issn 0301-0171Article

Epigenotype—phenotype correlations in Silver—Russell syndromeWAKELING, E. L; ABU AMERO, S; MOORE, G. E et al.Journal of medical genetics. 2010, Vol 47, Num 11, pp 760-768, issn 0022-2593, 9 p.Article

Catecholaminergic polymorphic ventricular tachycardia : RYR2 mutations, bradycardia, and follow up of the patientsPOSTMA, A. V; DENJOY, I; WILDE, A. A. M et al.Journal of medical genetics. 2005, Vol 42, Num 11, pp 863-870, issn 0022-2593, 8 p.Article

Homozygous premature truncation of the HERG protein : The human HERG knockoutHOORNTJE, T; ALDERS, M; VAN TINTELEN, P et al.Circulation (New York, N.Y.). 1999, Vol 100, Num 12, pp 1264-1267, issn 0009-7322Article

An integrated physical map of 210 markers assigned to the short arm of human chromosome 11REDEKER, E; HOOVERS, J. M. N; VISSER, J et al.Genomics (San Diego, Calif.). 1994, Vol 21, Num 3, pp 538-550, issn 0888-7543Article

Frequency of WT1 and 11p15 constitutional aberrations and phenotypic correlation in childhood Wilms tumour patientsSEGERS, H; KERSSEBOOM, R; ALDERS, M et al.European journal of cancer (1990). 2012, Vol 48, Num 17, pp 3249-3256, issn 0959-8049, 8 p.Article

Growth regulation of extraembryonic tissues the effect of genomic imprinting on development of the placentaOUDEJANS, C; WESTERMAN, B; VAN ELK, E et al.European journal of obstetrics, gynecology, and reproductive biology. 1997, Vol 75, Num 1, pp 29-32, issn 0301-2115Article

The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblastsALDERS, M; HODGES, M; LITTLE, P et al.Human molecular genetics (Print). 1997, Vol 6, Num 6, pp 859-867, issn 0964-6906Article

Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3REDEKER, E; ALDERS, M; HOOVERS, J. M. N et al.Cytogenetics and cell genetics. 1995, Vol 68, Num 3-4, pp 222-225, issn 0301-0171Conference Paper

(1-3)-β-glucan synthesis of Neurospora crassaJABRI, E; QUIGLEY, D. R; ALDERS, M et al.Current microbiology (Print). 1989, Vol 19, Num 3, pp 153-161, issn 0343-8651Article