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B B De Vries

Showing results (1-10 of 23) with videos related to

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Journal of Medical Genetics|July 25, 1998
The fragile X syndromeB B de Vries, D J Halley, B A Oostra, et al.
Clinical Dysmorphology|April 20, 2001
Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delayB B de Vries, W G van'tHoff, R A Surtees, et al.
Journal of Medical Genetics|March 2, 1999
Dilemmas in counselling females with the fragile X syndromeB B de Vries, H M van den Boer-van den Berg, M F Niermeijer, et al.
American Journal of Human Genetics|January 13, 2000
Benign hereditary chorea of early onset maps to chromosome 14qB B de Vries, W F Arts, G J Breedveld, et al.
American Journal of Medical Genetics|March 17, 2001
Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13)B B de Vries, M Lees, S J Knight, et al.
Journal of Medical Genetics|December 10, 1997
DNA testing for fragile X syndrome: implications for parents and familyM A van Rijn, B B de Vries, A Tibben, et al.
Clinical Genetics|January 10, 2001
A boy with a submicroscopic 22qter deletion, general overgrowth and features suggestive of FG syndromeB B de Vries, M Bitner-Glindzicz, S J Knight, et al.
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.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|July 25, 1998
The fragile X syndromeB B de Vries, D J Halley, B A Oostra, et al.
Clinical Dysmorphology|April 20, 2001
Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delayB B de Vries, W G van'tHoff, R A Surtees, et al.
Journal of Medical Genetics|March 2, 1999
Dilemmas in counselling females with the fragile X syndromeB B de Vries, H M van den Boer-van den Berg, M F Niermeijer, et al.
American Journal of Human Genetics|January 13, 2000
Benign hereditary chorea of early onset maps to chromosome 14qB B de Vries, W F Arts, G J Breedveld, et al.
American Journal of Medical Genetics|March 17, 2001
Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13)B B de Vries, M Lees, S J Knight, et al.
Journal of Medical Genetics|December 10, 1997
DNA testing for fragile X syndrome: implications for parents and familyM A van Rijn, B B de Vries, A Tibben, et al.
Clinical Genetics|January 10, 2001
A boy with a submicroscopic 22qter deletion, general overgrowth and features suggestive of FG syndromeB B de Vries, M Bitner-Glindzicz, S J Knight, et al.
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.
Pageof 3