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D Smeets

Showing results (1-10 of 52) with videos related to

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American Journal of Human Genetics|August 1, 1990
Genetic determination of fragile-site expressionD Smeets, A Arets
Mutation Research|June 1, 1989
Familial and individual variation in chromosome fragilityD Smeets, A Verhagen, T Hustinx
Nanoscale Research Letters|July 24, 2010
The Influence of an Adsorbate Layer on Adatom Diffusion and Island Nucleation: Fe on Si(111)-√3×√3-AuK Paredis, D Smeets, A Vantomme
Nanotechnology|May 7, 2009
Iron silicide nanostructure formation on Au induced superstructures on Si(111)K Paredis, D Smeets, A Vantomme
Genetic Counseling (Geneva, Switzerland)|April 30, 2009
A novel duplication of chromosome (13)(q14.1q21.3) in a patient with mental retardation and microcephalyW Verhoeven, M Ruiter, J Egger, et al.
Annales De Genetique|January 1, 1996
Another patient with a deletion 14q11.2q13L Govaerts, J Toorman, M V Blij-Philipsen, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 13, 1999
[Trisomy 9p: a clinical picture and the importance of examining the family]C van Ravenswaaij-Arts, E van der Looij, D Smeets
Human Genetics|September 1, 1996
Anesthesiologic problems in Williams syndrome: the CACNL2A locus is not involvedI Mammi, D E Iles, D Smeets, et al.
Human Genetics|March 1, 1987
Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19qU Friedrich, H Brunner, D Smeets, et al.
American Journal of Medical Genetics|April 1, 1992
High prevalence of the fra(X) syndrome cannot be explained by a high mutation rateA Smits, D Smeets, B Hamel, et al.
Pageof 6

Showing results (1-10 of 52) with videos related to

Sort By:
Pageof 6
American Journal of Human Genetics|August 1, 1990
Genetic determination of fragile-site expressionD Smeets, A Arets
Mutation Research|June 1, 1989
Familial and individual variation in chromosome fragilityD Smeets, A Verhagen, T Hustinx
Nanoscale Research Letters|July 24, 2010
The Influence of an Adsorbate Layer on Adatom Diffusion and Island Nucleation: Fe on Si(111)-√3×√3-AuK Paredis, D Smeets, A Vantomme
Nanotechnology|May 7, 2009
Iron silicide nanostructure formation on Au induced superstructures on Si(111)K Paredis, D Smeets, A Vantomme
Genetic Counseling (Geneva, Switzerland)|April 30, 2009
A novel duplication of chromosome (13)(q14.1q21.3) in a patient with mental retardation and microcephalyW Verhoeven, M Ruiter, J Egger, et al.
Annales De Genetique|January 1, 1996
Another patient with a deletion 14q11.2q13L Govaerts, J Toorman, M V Blij-Philipsen, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 13, 1999
[Trisomy 9p: a clinical picture and the importance of examining the family]C van Ravenswaaij-Arts, E van der Looij, D Smeets
Human Genetics|September 1, 1996
Anesthesiologic problems in Williams syndrome: the CACNL2A locus is not involvedI Mammi, D E Iles, D Smeets, et al.
Human Genetics|March 1, 1987
Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19qU Friedrich, H Brunner, D Smeets, et al.
American Journal of Medical Genetics|April 1, 1992
High prevalence of the fra(X) syndrome cannot be explained by a high mutation rateA Smits, D Smeets, B Hamel, et al.
Pageof 6