D F Smeets|J M Scheres|T W Hustinx - JoVE Visualize

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Immunodeficiency|January 1, 1993

Variants of Nijmegen breakage syndrome and ataxia telangiectasiaC M Weemaes, D F Smeets, M Horstink, et al.

Cytogenetics and Cell Genetics|January 1, 1986

Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie diseaseA Gal, B Wieringa, D F Smeets, et al.

Human Genetics|August 1, 1987

Absence of Y-specific DNA sequences in human 46,XX true hermaphrodites and in 45,X mixed gonadal dysgenesisF Waibel, G Scherer, M Fraccaro, et al.

American Journal of Medical Genetics|April 1, 1992

Penetrance estimate of the fra(X) gene using Pointer versus direct estimateA F de Haan, A P Smits, D F Smeets, et al.

Journal of Medical Genetics|October 1, 1994

Down-Turner syndrome: case report and reviewG J Van Buggenhout, B C Hamel, J C Trommelen, 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 1qJ M Scheres, J M de Pater, P Stoutenbeek, et al.

Genetic Counseling (Geneva, Switzerland)|October 24, 2000

Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17pJ M De Pater, J P Van Tintelen, R Stigter, et al.

Clinical Genetics|June 1, 1978

2:2 and 3:1 meiotic disjunctions in a carrier of a reciprocal 10/14 translocationJ 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 diseaseA 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 speciesD H Waalkens, H F Joosten, R D Taalman, et al.

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Showing results (41-50 of 92) with videos related to

Sort By:

Pageof 10

Immunodeficiency|January 1, 1993

Variants of Nijmegen breakage syndrome and ataxia telangiectasiaC M Weemaes, D F Smeets, M Horstink, et al.

Cytogenetics and Cell Genetics|January 1, 1986

Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie diseaseA Gal, B Wieringa, D F Smeets, et al.

Human Genetics|August 1, 1987

Absence of Y-specific DNA sequences in human 46,XX true hermaphrodites and in 45,X mixed gonadal dysgenesisF Waibel, G Scherer, M Fraccaro, et al.

American Journal of Medical Genetics|April 1, 1992

Penetrance estimate of the fra(X) gene using Pointer versus direct estimateA F de Haan, A P Smits, D F Smeets, et al.

Journal of Medical Genetics|October 1, 1994

Down-Turner syndrome: case report and reviewG J Van Buggenhout, B C Hamel, J C Trommelen, 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 1qJ M Scheres, J M de Pater, P Stoutenbeek, et al.

Genetic Counseling (Geneva, Switzerland)|October 24, 2000

Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17pJ M De Pater, J P Van Tintelen, R Stigter, et al.

Clinical Genetics|June 1, 1978

2:2 and 3:1 meiotic disjunctions in a carrier of a reciprocal 10/14 translocationJ 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 diseaseA 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 speciesD H Waalkens, H F Joosten, R D Taalman, et al.

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