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B B de Vries

Showing results (11-20 of 27) with videos related to

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Human Genetics|December 18, 1998
Screening with the FMR1 protein test among mentally retarded malesB B de Vries, S Mohkamsing, A M van den Ouweland, et al.
American Journal of Medical Genetics|August 9, 1996
The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28% of the cellsE de Graaff, B B de Vries, R Willemsen, et al.
American Journal of Human Genetics|June 12, 1999
Noninvasive test for fragile X syndrome, using hair root analysisR Willemsen, B Anar, Y De Diego Otero, 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.
Human Molecular Genetics|January 1, 1994
Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11Y Q Wu, P Heutink, B B de Vries, 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.
Journal of Medical Genetics|October 1, 1995
General overgrowth in the fragile X syndrome: variability in the phenotypic expression of the FMR1 gene mutationB B de Vries, H Robinson, I Stolte-Dijkstra, 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|June 30, 2000
Screening for the fragile X syndrome among the mentally retarded: a clinical study. The Collaborative Fragile X Study GroupB B de Vries, S Mohkamsing, A M van den Ouweland, et al.
Journal of Medical Genetics|December 1, 1996
Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X familyB B de Vries, C C Jansen, A A Duits, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Human Genetics|December 18, 1998
Screening with the FMR1 protein test among mentally retarded malesB B de Vries, S Mohkamsing, A M van den Ouweland, et al.
American Journal of Medical Genetics|August 9, 1996
The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28% of the cellsE de Graaff, B B de Vries, R Willemsen, et al.
American Journal of Human Genetics|June 12, 1999
Noninvasive test for fragile X syndrome, using hair root analysisR Willemsen, B Anar, Y De Diego Otero, 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.
Human Molecular Genetics|January 1, 1994
Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11Y Q Wu, P Heutink, B B de Vries, 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.
Journal of Medical Genetics|October 1, 1995
General overgrowth in the fragile X syndrome: variability in the phenotypic expression of the FMR1 gene mutationB B de Vries, H Robinson, I Stolte-Dijkstra, 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|June 30, 2000
Screening for the fragile X syndrome among the mentally retarded: a clinical study. The Collaborative Fragile X Study GroupB B de Vries, S Mohkamsing, A M van den Ouweland, et al.
Journal of Medical Genetics|December 1, 1996
Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X familyB B de Vries, C C Jansen, A A Duits, et al.
Pageof 3