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J M Scheres

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Clinical 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 Scheres
American Journal of Medical Genetics|January 1, 1979
Partial trisomy of chromosome 1 resulting from a complex maternal rearrangement of chromosomes 1, 5, and 6T W Hustinx, F A Nabben, J M Scheres
Human Genetics|March 1, 1986
The most common fragile site in man is 3p14D F Smeets, J M Scheres, T W Hustinx
Cancer 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.
Lancet (London, England)|August 29, 1981
Rapid diagnostic test for ataxia telangiectasiaN G Jaspers, J M Scheres, J De Wit, et al.
Experimental Cell Research|October 15, 1977
"Reverse" differential staining of sister chromatidsJ M Scheres, T W Hustinx, F J Rutten, et al.
British Journal of Haematology|March 1, 1974
Trisomy-9 in the bone marrow of a patient with acute myelomonoblastic leukaemiaF J Rutten, T W Hustinx, J M Scheres, et al.
Cytogenetics and Cell Genetics|January 1, 1986
Heterochromatin in the chromosomes of the gorilla: characterization with distamycin A/DAPI, D287/170, chromomycin A3, quinacrine, and 5-azacytidineM Schmid, T Haaf, G Ott, 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 7

Showing results (21-30 of 65) with videos related to

Sort By:
Pageof 7
Clinical 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 Scheres
American Journal of Medical Genetics|January 1, 1979
Partial trisomy of chromosome 1 resulting from a complex maternal rearrangement of chromosomes 1, 5, and 6T W Hustinx, F A Nabben, J M Scheres
Human Genetics|March 1, 1986
The most common fragile site in man is 3p14D F Smeets, J M Scheres, T W Hustinx
Cancer 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.
Lancet (London, England)|August 29, 1981
Rapid diagnostic test for ataxia telangiectasiaN G Jaspers, J M Scheres, J De Wit, et al.
Experimental Cell Research|October 15, 1977
"Reverse" differential staining of sister chromatidsJ M Scheres, T W Hustinx, F J Rutten, et al.
British Journal of Haematology|March 1, 1974
Trisomy-9 in the bone marrow of a patient with acute myelomonoblastic leukaemiaF J Rutten, T W Hustinx, J M Scheres, et al.
Cytogenetics and Cell Genetics|January 1, 1986
Heterochromatin in the chromosomes of the gorilla: characterization with distamycin A/DAPI, D287/170, chromomycin A3, quinacrine, and 5-azacytidineM Schmid, T Haaf, G Ott, 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 7