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Showing results (91-100 of 108) with videos related to

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Human Molecular Genetics|October 1, 1995
Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the diseaseS Bione, K Small, V M Aksmanovic, et al.
American Journal of Human Genetics|March 1, 1996
FMR1 in global populationsC B Kunst, C Zerylnick, L Karickhoff, et al.
American Journal of Human Genetics|August 1, 1992
Further localization of X-linked hydrocephalus in the chromosomal region Xq28P J Willems, L Vits, P Raeymaekers, et al.
Science (New York, N.Y.)|June 21, 1991
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)nE J Kremer, M Pritchard, M Lynch, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 30, 1998
A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergenceH H Chou, H Takematsu, S Diaz, et al.
Human Molecular Genetics|October 1, 1994
Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomesA M van den Ouweland, W H Deelen, C B Kunst, et al.
Genomics|June 1, 1992
Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panelH Traupe, A M van den Ouweland, B A van Oost, et al.
American Journal of Human Genetics|March 1, 1991
Assignment of Emery-Dreifuss muscular dystrophy to the distal region of Xq28: the results of a collaborative studyG G Consalez, N S Thomas, C L Stayton, 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.
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.
Pageof 11

Showing results (91-100 of 108) with videos related to

Sort By:
Pageof 11
Human Molecular Genetics|October 1, 1995
Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the diseaseS Bione, K Small, V M Aksmanovic, et al.
American Journal of Human Genetics|March 1, 1996
FMR1 in global populationsC B Kunst, C Zerylnick, L Karickhoff, et al.
American Journal of Human Genetics|August 1, 1992
Further localization of X-linked hydrocephalus in the chromosomal region Xq28P J Willems, L Vits, P Raeymaekers, et al.
Science (New York, N.Y.)|June 21, 1991
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)nE J Kremer, M Pritchard, M Lynch, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 30, 1998
A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergenceH H Chou, H Takematsu, S Diaz, et al.
Human Molecular Genetics|October 1, 1994
Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomesA M van den Ouweland, W H Deelen, C B Kunst, et al.
Genomics|June 1, 1992
Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panelH Traupe, A M van den Ouweland, B A van Oost, et al.
American Journal of Human Genetics|March 1, 1991
Assignment of Emery-Dreifuss muscular dystrophy to the distal region of Xq28: the results of a collaborative studyG G Consalez, N S Thomas, C L Stayton, 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.
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.
Pageof 11