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Humangenetik
|
January 1, 1974
A presumptive tetrasomy for the short arm of chromosome 9
F J Rutten, J M Scheres, T W Hustinx, et al.
Clinical Genetics
|
January 1, 1974
Trisomy for the short arm of chromosome No. 10
T W Hustinx, B G Ter Haar, J M Scheres, et al.
Human Genetics
|
July 12, 1978
15/17 translocation in acute promyelocytic leukaemia
J 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 child
T 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 constitution
J 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 Syndrome
R 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 cases
J M Scheres, T W Hustinx, J P Geraedts, et al.
Clinical Neurology and Neurosurgery
|
January 1, 1982
X-linked congenital hydrocephalus
W 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 rearrangements
T W Hustinx, J M Scheres, C M Weemaes, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 47) with videos related to
Sort By:
Page
of 5
Humangenetik
|
January 1, 1974
A presumptive tetrasomy for the short arm of chromosome 9
F J Rutten, J M Scheres, T W Hustinx, et al.
Clinical Genetics
|
January 1, 1974
Trisomy for the short arm of chromosome No. 10
T W Hustinx, B G Ter Haar, J M Scheres, et al.
Human Genetics
|
July 12, 1978
15/17 translocation in acute promyelocytic leukaemia
J 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 child
T 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 constitution
J 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 Syndrome
R 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 cases
J M Scheres, T W Hustinx, J P Geraedts, et al.
Clinical Neurology and Neurosurgery
|
January 1, 1982
X-linked congenital hydrocephalus
W 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 rearrangements
T W Hustinx, J M Scheres, C M Weemaes, et al.
Page
of 5