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Nature Genetics
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November 1, 1994
Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE
J 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 syndrome
C 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 syndrome
A 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 paradox
Y H Fu, D P Kuhl, A Pizzuti, et al.
Human Molecular Genetics
|
April 1, 1993
Alternative splicing in the fragile X gene FMR1
A 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 sperm
E Reyniers, L Vits, K De Boulle, et al.
American Journal of Medical Genetics
|
April 1, 1992
Intragenic probe used for diagnostics in fragile X families
A 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 retardation
K De Boulle, A J Verkerk, E Reyniers, et al.
Oncogene
|
January 9, 1997
Unique expression patterns of H19 in human testicular cancers of different etiology
A 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 adults
M C Mostert, A J Verkerk, M van de Pol, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 22) with videos related to
Sort By:
Page
of 3
Nature Genetics
|
November 1, 1994
Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE
J 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 syndrome
C 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 syndrome
A 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 paradox
Y H Fu, D P Kuhl, A Pizzuti, et al.
Human Molecular Genetics
|
April 1, 1993
Alternative splicing in the fragile X gene FMR1
A 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 sperm
E Reyniers, L Vits, K De Boulle, et al.
American Journal of Medical Genetics
|
April 1, 1992
Intragenic probe used for diagnostics in fragile X families
A 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 retardation
K De Boulle, A J Verkerk, E Reyniers, et al.
Oncogene
|
January 9, 1997
Unique expression patterns of H19 in human testicular cancers of different etiology
A 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 adults
M C Mostert, A J Verkerk, M van de Pol, et al.
Page
of 3