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T W Hustinx

Showing results (21-30 of 47) with videos related to

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Humangenetik|January 1, 1974
A presumptive tetrasomy for the short arm of chromosome 9F J Rutten, J M Scheres, T W Hustinx, et al.
Clinical Genetics|January 1, 1974
Trisomy for the short arm of chromosome No. 10T W Hustinx, B G Ter Haar, J M Scheres, 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.
Journal of Mental Deficiency Research|March 1, 1975
Self-mutilation in a case of 49, XXXXY chromosomal constitutionJ J Korten, A van Dorp, T W Hustinx, 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.
Nederlands Tijdschrift Voor Geneeskunde|September 14, 1985
[A Dutch chromosome abnormality in myelodysplasia?]J M Scheres, T W Hustinx, J P Geraedts, 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.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
Humangenetik|January 1, 1974
A presumptive tetrasomy for the short arm of chromosome 9F J Rutten, J M Scheres, T W Hustinx, et al.
Clinical Genetics|January 1, 1974
Trisomy for the short arm of chromosome No. 10T W Hustinx, B G Ter Haar, J M Scheres, 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.
Journal of Mental Deficiency Research|March 1, 1975
Self-mutilation in a case of 49, XXXXY chromosomal constitutionJ J Korten, A van Dorp, T W Hustinx, 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.
Nederlands Tijdschrift Voor Geneeskunde|September 14, 1985
[A Dutch chromosome abnormality in myelodysplasia?]J M Scheres, T W Hustinx, J P Geraedts, 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.
Pageof 5