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A J Verkerk

Showing results (11-20 of 22) with videos related to

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Nature Genetics|November 1, 1994
Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXEJ E Parrish, B A Oostra, A J Verkerk, et al.
Nature|June 24, 1993
Characterization and localization of the FMR-1 gene product associated with fragile X syndromeC Verheij, C E Bakker, E de Graaff, et al.
Cell|May 31, 1991
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromeA J Verkerk, M Pieretti, J S Sutcliffe, et al.
Cell|December 30, 1991
Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradoxY H Fu, D P Kuhl, A Pizzuti, et al.
Human Molecular Genetics|April 1, 1993
Alternative splicing in the fragile X gene FMR1A J Verkerk, E de Graaff, K De Boulle, et al.
Nature Genetics|June 1, 1993
The full mutation in the FMR-1 gene of male fragile X patients is absent in their spermE Reyniers, L Vits, K De Boulle, et al.
American Journal of Medical Genetics|April 1, 1992
Intragenic probe used for diagnostics in fragile X familiesA J Verkerk, B B deVries, M F Niermeijer, et al.
Nature Genetics|January 1, 1993
A point mutation in the FMR-1 gene associated with fragile X mental retardationK De Boulle, A J Verkerk, E Reyniers, et al.
Oncogene|January 9, 1997
Unique expression patterns of H19 in human testicular cancers of different etiologyA J Verkerk, I Ariel, M C Dekker, et al.
Oncogene|June 19, 1998
Identification of the critical region of 12p over-representation in testicular germ cell tumors of adolescents and adultsM C Mostert, A J Verkerk, M van de Pol, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Nature Genetics|November 1, 1994
Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXEJ E Parrish, B A Oostra, A J Verkerk, et al.
Nature|June 24, 1993
Characterization and localization of the FMR-1 gene product associated with fragile X syndromeC Verheij, C E Bakker, E de Graaff, et al.
Cell|May 31, 1991
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromeA J Verkerk, M Pieretti, J S Sutcliffe, et al.
Cell|December 30, 1991
Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradoxY H Fu, D P Kuhl, A Pizzuti, et al.
Human Molecular Genetics|April 1, 1993
Alternative splicing in the fragile X gene FMR1A J Verkerk, E de Graaff, K De Boulle, et al.
Nature Genetics|June 1, 1993
The full mutation in the FMR-1 gene of male fragile X patients is absent in their spermE Reyniers, L Vits, K De Boulle, et al.
American Journal of Medical Genetics|April 1, 1992
Intragenic probe used for diagnostics in fragile X familiesA J Verkerk, B B deVries, M F Niermeijer, et al.
Nature Genetics|January 1, 1993
A point mutation in the FMR-1 gene associated with fragile X mental retardationK De Boulle, A J Verkerk, E Reyniers, et al.
Oncogene|January 9, 1997
Unique expression patterns of H19 in human testicular cancers of different etiologyA J Verkerk, I Ariel, M C Dekker, et al.
Oncogene|June 19, 1998
Identification of the critical region of 12p over-representation in testicular germ cell tumors of adolescents and adultsM C Mostert, A J Verkerk, M van de Pol, et al.
Pageof 3