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Tijdschrift Voor Kindergeneeskunde|October 1, 1988
[Immunodeficiency and chromosome instability]C M Weemaes, J A Bakkeren, T W Hustinx, et al.Genetic Counseling (Geneva, Switzerland)|October 24, 2000
Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17pJ M De Pater, J P Van Tintelen, R Stigter, et al.Annales De Genetique|March 1, 1978
A case of partial 9p monosomy with some unusual clinical featuresF J Rutten, T W Hustinx, A A Dunk-Tillemans, et al.British Journal of Haematology|September 1, 1977
Monosomy 7 in two patients with a myeloproliferative disorderG Boetius, T W Hustinx, A P Smits, et al.Clinical Genetics|June 1, 1978
2:2 and 3:1 meiotic disjunctions in a carrier of a reciprocal 10/14 translocationJ M Scheres, W J Hustinx, B G Ter Haar, et al.American Journal of Medical Genetics|February 13, 2001
Variegated aneuploidy related to premature centromere division (PCD) is expressed in vivo and is a cancer-prone diseaseA Plaja, T Vendrell, D Smeets, et al.Toxicology Letters|January 1, 1981
Sister-chromatid exchanges induced in vitro by cyclophosphamide without exogenous metabolic activation in lymphocytes from three mammalian speciesD H Waalkens, H F Joosten, R D Taalman, et al.Cytogenetics and Cell Genetics|January 1, 1996
The gene (PTPN13) encoding the protein tyrosine phosphatase PTP-BL/PTP-BAS is located in mouse chromosome region 5E/F and human chromosome region 4q21A M van den Maagdenberg, D Olde Weghuis, J Rijss, et al.Journal of Medical Genetics|June 1, 1975
A mentally retarded child with a translocation involving chromosomes 12 and 19T W Histinx, F J Gabreëls, F J Rutten, et al.Human Molecular Genetics|November 1, 1995
A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 geneY J de Kok, G F Merkx, S M van der Maarel, et al.Pageof 6