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S T Warren

Showing results (81-90 of 108) with videos related to

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Genomics|April 1, 1992
Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28G G Consalez, C L Stayton, N B Freimer, et al.
Somatic Cell Genetics|March 1, 1981
Isolation and characterization of a UV-sensitive hypermutable aphidicolin-resistant Chinese hamster cell lineC C Chang, J A Boezi, S T Warren, et al.
Nature Genetics|July 1, 1993
Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeatC T Ashley, J S Sutcliffe, C B Kunst, et al.
Journal of Medical Genetics|September 22, 2001
Microdeletion in the FMR-1 gene: an apparent null allele using routine clinical PCR amplificationM R Hegde, B Chong, M Fawkner, et al.
Nature Genetics|November 1, 1992
Human genes containing polymorphic trinucleotide repeatsG J Riggins, L K Lokey, J L Chastain, et al.
Science (New York, N.Y.)|May 24, 1991
Fragile X genotype characterized by an unstable region of DNAS Yu, M Pritchard, E Kremer, et al.
Nature Genetics|February 1, 1997
Characterization of the full fragile X syndrome mutation in fetal gametesH E Malter, J C Iber, R Willemsen, et al.
American Journal of Human Genetics|January 1, 1991
Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA)F Rousseau, A Vincent, S Rivella, et al.
Genomics|August 1, 1993
Actin-binding protein (ABP-280) filamin gene (FLN) maps telomeric to the color vision locus (R/GCP) and centromeric to G6PD in Xq28J B Gorlin, E Henske, S T Warren, et al.
Journal of Medical Genetics|March 19, 2002
A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotypeJ Tarleton, A Kenneson, A K Taylor, et al.
Pageof 11

Showing results (81-90 of 108) with videos related to

Sort By:
Pageof 11
Genomics|April 1, 1992
Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28G G Consalez, C L Stayton, N B Freimer, et al.
Somatic Cell Genetics|March 1, 1981
Isolation and characterization of a UV-sensitive hypermutable aphidicolin-resistant Chinese hamster cell lineC C Chang, J A Boezi, S T Warren, et al.
Nature Genetics|July 1, 1993
Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeatC T Ashley, J S Sutcliffe, C B Kunst, et al.
Journal of Medical Genetics|September 22, 2001
Microdeletion in the FMR-1 gene: an apparent null allele using routine clinical PCR amplificationM R Hegde, B Chong, M Fawkner, et al.
Nature Genetics|November 1, 1992
Human genes containing polymorphic trinucleotide repeatsG J Riggins, L K Lokey, J L Chastain, et al.
Science (New York, N.Y.)|May 24, 1991
Fragile X genotype characterized by an unstable region of DNAS Yu, M Pritchard, E Kremer, et al.
Nature Genetics|February 1, 1997
Characterization of the full fragile X syndrome mutation in fetal gametesH E Malter, J C Iber, R Willemsen, et al.
American Journal of Human Genetics|January 1, 1991
Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA)F Rousseau, A Vincent, S Rivella, et al.
Genomics|August 1, 1993
Actin-binding protein (ABP-280) filamin gene (FLN) maps telomeric to the color vision locus (R/GCP) and centromeric to G6PD in Xq28J B Gorlin, E Henske, S T Warren, et al.
Journal of Medical Genetics|March 19, 2002
A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotypeJ Tarleton, A Kenneson, A K Taylor, et al.
Pageof 11