H J Eussen - JoVE Visualize

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Human Genetics|January 5, 2001

Interchromosomal insertions. Identification of five cases and a reviewJ O Van Hemel, H J Eussen

Prenatal Diagnosis|September 1, 1993

Application of fluorescent in situ hybridization for 'de novo' anomalies in prenatal diagnosisD Van Opstal, H J Eussen, J O Van Hemel, et al.

Clinical Genetics|April 22, 2004

Deletion of the TWIST gene in a large five-generation familyI M De Heer, A J M Hoogeboom, H J Eussen, et al.

Genomics|June 18, 2003

CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorderAnnemieke J M H Verkerk, Carol A Mathews, Marijke Joosse, et al.

Prenatal Diagnosis|December 13, 2006

FISH analysis of 15 chromosomes in human day 4 and 5 preimplantation embryos: the added value of extended aneuploidy detectionE B Baart, I van den Berg, E Martini, et al.

American Journal of Medical Genetics|September 1, 1991

DNA analysis in patients with lissencephaly type I and other cortical dysplasiasB A Oostra, J F de Rijk-van Andel, H J Eussen, et al.

American Journal of Medical Genetics. Part A|August 12, 2003

Isolated postaxial polydactyly type B with mosaicism of a submicroscopic unbalanced translocation leading to an extended phenotype in offspringRobert-Jan H Galjaard, Herma C van der Linde, Bert H J Eussen, et al.

Journal of Medical Genetics|December 4, 2009

Phenotype-genotype correlation in a familial IGF1R microdeletion caseD C M Veenma, H J Eussen, L C P Govaerts, et al.

European Journal of Medical Genetics|June 13, 2017

Postzygotic telomere capture causes segmental UPD, duplication and deletion of chromosome 8p in a patient with intellectual disability and obesityJeroen Knijnenburg, Madiek E W Uytdewilligen, Daniella A C M van Hassel, et al.

Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|February 19, 2002

Quantification of MYCN, DDX1, and NAG gene copy number in neuroblastoma using a real-time quantitative PCR assayKatleen De Preter, Frank Speleman, Valérie Combaret, et al.

Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:

Pageof 2

Human Genetics|January 5, 2001

Interchromosomal insertions. Identification of five cases and a reviewJ O Van Hemel, H J Eussen

Prenatal Diagnosis|September 1, 1993

Application of fluorescent in situ hybridization for 'de novo' anomalies in prenatal diagnosisD Van Opstal, H J Eussen, J O Van Hemel, et al.

Clinical Genetics|April 22, 2004

Deletion of the TWIST gene in a large five-generation familyI M De Heer, A J M Hoogeboom, H J Eussen, et al.

Genomics|June 18, 2003

CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorderAnnemieke J M H Verkerk, Carol A Mathews, Marijke Joosse, et al.

Prenatal Diagnosis|December 13, 2006

FISH analysis of 15 chromosomes in human day 4 and 5 preimplantation embryos: the added value of extended aneuploidy detectionE B Baart, I van den Berg, E Martini, et al.

American Journal of Medical Genetics|September 1, 1991

DNA analysis in patients with lissencephaly type I and other cortical dysplasiasB A Oostra, J F de Rijk-van Andel, H J Eussen, et al.

American Journal of Medical Genetics. Part A|August 12, 2003

Isolated postaxial polydactyly type B with mosaicism of a submicroscopic unbalanced translocation leading to an extended phenotype in offspringRobert-Jan H Galjaard, Herma C van der Linde, Bert H J Eussen, et al.

Journal of Medical Genetics|December 4, 2009

Phenotype-genotype correlation in a familial IGF1R microdeletion caseD C M Veenma, H J Eussen, L C P Govaerts, et al.

European Journal of Medical Genetics|June 13, 2017

Postzygotic telomere capture causes segmental UPD, duplication and deletion of chromosome 8p in a patient with intellectual disability and obesityJeroen Knijnenburg, Madiek E W Uytdewilligen, Daniella A C M van Hassel, et al.

Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|February 19, 2002

Quantification of MYCN, DDX1, and NAG gene copy number in neuroblastoma using a real-time quantitative PCR assayKatleen De Preter, Frank Speleman, Valérie Combaret, et al.

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