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Tijdschrift Voor Kindergeneeskunde|August 1, 1986
[Down's syndrome in the Netherlands]T W Hustinx, J M Scheres, J P Geraedts, et al.Human Genetics|July 12, 1978
15/17 translocation in acute promyelocytic leukaemiaJ M Scheres, T W Hustinx, G A de Vaan, et al.Cancer|October 1, 1983
Malignant histiocytosis. Clinical and cytogenetic studies in a newborn and a childT J Schouten, T W Hustinx, J M Scheres, et al.Mutation Research|February 1, 1983
Hypersensitivity to ionizing radiation, in vitro, in a new chromosomal breakage disorder, the Nijmegen Breakage SyndromeR D Taalman, N G Jaspers, J M Scheres, et al.Cancer Genetics and Cytogenetics|November 1, 1985
Translocation 1;7 in hematologic disorders: a brief review of 22 casesJ M Scheres, T W Hustinx, J P Geraedts, et al.Clinical Neurology and Neurosurgery|January 1, 1982
X-linked congenital hydrocephalusW O Renier, B G Ter Haar, J L Slooff, et al.Human Genetics|June 19, 1979
Karyotype instability with multiple 7/14 and 7/7 rearrangementsT W Hustinx, J M Scheres, C M Weemaes, et al.Tijdschrift Voor Kindergeneeskunde|October 1, 1988
[Immunodeficiency and chromosome instability]C M Weemaes, J A Bakkeren, T W Hustinx, 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.Pageof 3