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Cancer Genetics and Cytogenetics|January 1, 1986
Possible involvement of unstable sites on chromosomes 7 and 14 in human cancerJ M Scheres, T W Hustinx, J M TrentHuman Genetics|February 1, 1980
Nomarski-optical studies of human chromosomes R-banded with barium hydroxideJ M Scheres, T W Hustinx, G F MerkxHuman Genetics|January 1, 1982
Prometaphase banding of human chromosomes with basic fuchsinJ M Scheres, G F Merkx, T W HustinxClinical Genetics|August 1, 1985
Heritable fragility at 11q13 and 12q13D F Smeets, J M Scheres, T W HustinxClinical Genetics|December 1, 1980
Habitual abortion and translocation (22q;22q): unexpected transmission from a mother to her phenotypically normal daughterV G Kirkels, T W Hustinx, J M ScheresHuman Genetics|March 1, 1986
The most common fragile site in man is 3p14D F Smeets, J M Scheres, T W HustinxHuman Genetics|November 10, 1977
A case of chronic myeloid leukemia with a translocation (12;22)(p13;q11)M van der Blij-Philipsen, W P Breed, T W HustinxCancer Genetics and Cytogenetics|May 1, 1986
Specific translocation t(1;3) in acute myelomonocytic leukemia: a further caseJ M Scheres, T W Hustinx, J G Haasjes, et al.Histochemistry|January 1, 1986
Demonstration of X chromatin in drumstick-like nuclear appendages of leukocytes by in situ hybridization on blood smearsP F Hochstenbach, J M Scheres, T W Hustinx, et al.Cancer|January 15, 1980
A case of AMMoL with 8/21 translocation and loss of the Y as probably secondary eventsT W Hustinx, J T Burghouts, J M Scheres, et al.Pageof 3