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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.
Cancer Genetics and Cytogenetics
|
November 24, 1999
Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas. Possible trisomic or tetrasomic zygote rescue in fetal teratoma with an additional isochromosome 1q
J M Scheres, J M de Pater, P Stoutenbeek, 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.
Tijdschrift Voor Kindergeneeskunde
|
October 1, 1988
[Immunodeficiency and chromosome instability]
C M Weemaes, J A Bakkeren, T W Hustinx, et al.
Genetic Counseling (Geneva, Switzerland)
|
October 24, 2000
Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17p
J M De Pater, J P Van Tintelen, R Stigter, et al.
Annales De Genetique
|
March 1, 1978
A case of partial 9p monosomy with some unusual clinical features
F J Rutten, T W Hustinx, A A Dunk-Tillemans, et al.
British Journal of Haematology
|
September 1, 1977
Monosomy 7 in two patients with a myeloproliferative disorder
G Boetius, T W Hustinx, A P Smits, et al.
Clinical Genetics
|
June 1, 1978
2:2 and 3:1 meiotic disjunctions in a carrier of a reciprocal 10/14 translocation
J M Scheres, W J Hustinx, B G Ter Haar, et al.
American Journal of Medical Genetics
|
February 13, 2001
Variegated aneuploidy related to premature centromere division (PCD) is expressed in vivo and is a cancer-prone disease
A Plaja, T Vendrell, D Smeets, et al.
Toxicology Letters
|
January 1, 1981
Sister-chromatid exchanges induced in vitro by cyclophosphamide without exogenous metabolic activation in lymphocytes from three mammalian species
D H Waalkens, H F Joosten, R D Taalman, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 65) with videos related to
Sort By:
Page
of 7
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.
Cancer Genetics and Cytogenetics
|
November 24, 1999
Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas. Possible trisomic or tetrasomic zygote rescue in fetal teratoma with an additional isochromosome 1q
J M Scheres, J M de Pater, P Stoutenbeek, 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.
Tijdschrift Voor Kindergeneeskunde
|
October 1, 1988
[Immunodeficiency and chromosome instability]
C M Weemaes, J A Bakkeren, T W Hustinx, et al.
Genetic Counseling (Geneva, Switzerland)
|
October 24, 2000
Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17p
J M De Pater, J P Van Tintelen, R Stigter, et al.
Annales De Genetique
|
March 1, 1978
A case of partial 9p monosomy with some unusual clinical features
F J Rutten, T W Hustinx, A A Dunk-Tillemans, et al.
British Journal of Haematology
|
September 1, 1977
Monosomy 7 in two patients with a myeloproliferative disorder
G Boetius, T W Hustinx, A P Smits, et al.
Clinical Genetics
|
June 1, 1978
2:2 and 3:1 meiotic disjunctions in a carrier of a reciprocal 10/14 translocation
J M Scheres, W J Hustinx, B G Ter Haar, et al.
American Journal of Medical Genetics
|
February 13, 2001
Variegated aneuploidy related to premature centromere division (PCD) is expressed in vivo and is a cancer-prone disease
A Plaja, T Vendrell, D Smeets, et al.
Toxicology Letters
|
January 1, 1981
Sister-chromatid exchanges induced in vitro by cyclophosphamide without exogenous metabolic activation in lymphocytes from three mammalian species
D H Waalkens, H F Joosten, R D Taalman, et al.
Page
of 7