J O van Hemel - JoVE Visualize

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Human Genetics|January 19, 1979

Partial trisomy 10q: a recognizable syndromeJ M Klep-de Pater, J B Bijlsma, H F de France, et al.

Prenatal Diagnosis|August 1, 1995

A chromosome 21-specific cosmid cocktail for the detection of chromosome 21 aberrations in interphase nucleiD van Opstal, J O van Hemel, B H Eussen, et al.

Cancer Genetics and Cytogenetics|January 1, 1987

Sister chromatid exchanges, hyperdiploidy and chromosomal rearrangements studied in cells from melanoma-prone individuals belonging to families with the dysplastic nevus syndromeN G Jaspers, E J Roza-de Jongh, I G Donselaar, et al.

Journal of Medical Genetics|September 1, 1993

Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotypeB B de Vries, J P Fryns, M G Butler, et al.

American Journal of Medical Genetics|October 26, 1999

Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14)B B de Vries, B H Eussen, O P van Diggelen, et al.

Human Reproduction (Oxford, England)|January 5, 2002

Genetic risk factors in infertile men with severe oligozoospermia and azoospermiaG R Dohle, D J J Halley, J O Van Hemel, et al.

American Journal of Medical Genetics|August 3, 2001

Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndromeC H Wouters, H J Meijers-Heijboer, B J Eussen, et al.

American Journal of Medical Genetics|July 15, 1994

DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 geneA M van den Ouweland, B B de Vries, P L Bakker, et al.

Journal of Medical Genetics|December 1, 1992

Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndromeE J Meijers-Heijboer, L A Sandkuijl, H G Brunner, et al.

European Journal of Human Genetics : EJHG|January 1, 1993

Mental status and fragile X expression in relation to FMR-1 gene mutationB B de Vries, A M Wiegers, E de Graaff, et al.

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Showing results (21-30 of 38) with videos related to

Sort By:

Pageof 4

Human Genetics|January 19, 1979

Partial trisomy 10q: a recognizable syndromeJ M Klep-de Pater, J B Bijlsma, H F de France, et al.

Prenatal Diagnosis|August 1, 1995

A chromosome 21-specific cosmid cocktail for the detection of chromosome 21 aberrations in interphase nucleiD van Opstal, J O van Hemel, B H Eussen, et al.

Cancer Genetics and Cytogenetics|January 1, 1987

Sister chromatid exchanges, hyperdiploidy and chromosomal rearrangements studied in cells from melanoma-prone individuals belonging to families with the dysplastic nevus syndromeN G Jaspers, E J Roza-de Jongh, I G Donselaar, et al.

Journal of Medical Genetics|September 1, 1993

Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotypeB B de Vries, J P Fryns, M G Butler, et al.

American Journal of Medical Genetics|October 26, 1999

Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14)B B de Vries, B H Eussen, O P van Diggelen, et al.

Human Reproduction (Oxford, England)|January 5, 2002

Genetic risk factors in infertile men with severe oligozoospermia and azoospermiaG R Dohle, D J J Halley, J O Van Hemel, et al.

American Journal of Medical Genetics|August 3, 2001

Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndromeC H Wouters, H J Meijers-Heijboer, B J Eussen, et al.

American Journal of Medical Genetics|July 15, 1994

DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 geneA M van den Ouweland, B B de Vries, P L Bakker, et al.

Journal of Medical Genetics|December 1, 1992

Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndromeE J Meijers-Heijboer, L A Sandkuijl, H G Brunner, et al.

European Journal of Human Genetics : EJHG|January 1, 1993

Mental status and fragile X expression in relation to FMR-1 gene mutationB B de Vries, A M Wiegers, E de Graaff, et al.

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