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T W Hustinx

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Human Genetics|March 1, 1986
The most common fragile site in man is 3p14D F Smeets, J M Scheres, T W Hustinx
Human 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 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.
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.
Lancet (London, England)|August 25, 1973
Acquired trisomy 9F J Rutten, T W Hustinx, M J Scheres, 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.
Annales De Genetique|December 1, 1974
Autosomal/heterosomal mixoploids: a report on two patients, a female with a 45, Z/47,XX plus 21 and a male with A 45,X/47,XY, plus 21 chromosome constitutionT W Hustinx, B G Haar, J M Scheres, et al.
Tijdschrift Voor Kindergeneeskunde|August 1, 1986
[Down's syndrome in the Netherlands]T W Hustinx, J M Scheres, J P Geraedts, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
Human Genetics|March 1, 1986
The most common fragile site in man is 3p14D F Smeets, J M Scheres, T W Hustinx
Human 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 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.
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.
Lancet (London, England)|August 25, 1973
Acquired trisomy 9F J Rutten, T W Hustinx, M J Scheres, 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.
Annales De Genetique|December 1, 1974
Autosomal/heterosomal mixoploids: a report on two patients, a female with a 45, Z/47,XX plus 21 and a male with A 45,X/47,XY, plus 21 chromosome constitutionT W Hustinx, B G Haar, J M Scheres, et al.
Tijdschrift Voor Kindergeneeskunde|August 1, 1986
[Down's syndrome in the Netherlands]T W Hustinx, J M Scheres, J P Geraedts, et al.
Pageof 5