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E Orye

Showing results (11-20 of 21) with videos related to

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Clinical Genetics|February 1, 1975
A new case of the trisomy 9P syndrome. Report of a patient with unusual chromosome findings (46,XX/47,XX, + i (9p) and a peculiar congenital heart defectE Orye, H Verhaaren, H Van Egmond, et al.
European Journal of Pediatrics|November 1, 1985
Meningeal leukaemia in the blastic phase of chronic granulocytic leukaemiaH Van Bever, Y Benoit, M J Delbeke, et al.
Clinical Genetics|November 1, 1975
The 9p- deletion syndrome. Report of a patient with a 46, XX, 9P- constitution due to a paternal t(9p-;15+) translocationE Orye, H Verhaaren, A M Van den Bogaert-Van Heesvelde
Science (New York, N.Y.)|July 27, 1973
Mucopolysaccharidosis: secondarily induced abnormal distribution of lysosomal isoenzymesJ A Kint, G Dacremont, D Carton, et al.
Journal De Genetique Humaine|January 1, 1985
Trisomy 10p, due to an unusual translocationE Orye, P Van Haesebrouck, R Van Coster, et al.
Journal of Medical Genetics|June 1, 1985
Extra Yq and partial monosomy 12p due to a Y;12 translocation in a boy with features of the 12p deletion syndromeE Orye, M Craen, G Laureys, et al.
British Heart Journal|July 1, 1988
Hypoplastic left heart syndrome and 45X karyotypeH van Egmond, E Orye, M Praet, et al.
Journal of Immunological Methods|June 10, 1983
A new, simple and rapid method for enumerating human T lymphocytes in full blood: the E. coli (ATCC 11303) rosette testE Orye, Y Benoit, L Roesbeke, et al.
Histochemistry|January 1, 1985
beta-D-N-acetylglucosaminidase, a new cytochemical marker of human lymphocyte subpopulationsE Orye, Y Benoit, L Roesbeke, et al.
Cancer Genetics and Cytogenetics|May 1, 1983
Pentasomy 21 characterizing spontaneously regressing congenital acute leukemiaH Van den Berghe, K Vermaelen, A Broeckaert-Van Orshoven, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Clinical Genetics|February 1, 1975
A new case of the trisomy 9P syndrome. Report of a patient with unusual chromosome findings (46,XX/47,XX, + i (9p) and a peculiar congenital heart defectE Orye, H Verhaaren, H Van Egmond, et al.
European Journal of Pediatrics|November 1, 1985
Meningeal leukaemia in the blastic phase of chronic granulocytic leukaemiaH Van Bever, Y Benoit, M J Delbeke, et al.
Clinical Genetics|November 1, 1975
The 9p- deletion syndrome. Report of a patient with a 46, XX, 9P- constitution due to a paternal t(9p-;15+) translocationE Orye, H Verhaaren, A M Van den Bogaert-Van Heesvelde
Science (New York, N.Y.)|July 27, 1973
Mucopolysaccharidosis: secondarily induced abnormal distribution of lysosomal isoenzymesJ A Kint, G Dacremont, D Carton, et al.
Journal De Genetique Humaine|January 1, 1985
Trisomy 10p, due to an unusual translocationE Orye, P Van Haesebrouck, R Van Coster, et al.
Journal of Medical Genetics|June 1, 1985
Extra Yq and partial monosomy 12p due to a Y;12 translocation in a boy with features of the 12p deletion syndromeE Orye, M Craen, G Laureys, et al.
British Heart Journal|July 1, 1988
Hypoplastic left heart syndrome and 45X karyotypeH van Egmond, E Orye, M Praet, et al.
Journal of Immunological Methods|June 10, 1983
A new, simple and rapid method for enumerating human T lymphocytes in full blood: the E. coli (ATCC 11303) rosette testE Orye, Y Benoit, L Roesbeke, et al.
Histochemistry|January 1, 1985
beta-D-N-acetylglucosaminidase, a new cytochemical marker of human lymphocyte subpopulationsE Orye, Y Benoit, L Roesbeke, et al.
Cancer Genetics and Cytogenetics|May 1, 1983
Pentasomy 21 characterizing spontaneously regressing congenital acute leukemiaH Van den Berghe, K Vermaelen, A Broeckaert-Van Orshoven, et al.
Pageof 3