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C Oudet

Showing results (21-30 of 37) with videos related to

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Human Molecular Genetics|November 1, 1992
Two hot spots of recombination in the DMD gene correlate with the deletion prone regionsC Oudet, A Hanauer, P Clemens, et al.
Human Molecular Genetics|May 1, 1993
Dinucleotide repeat polymorphism at Xq26.1 (DXS1114)C Weber, C Oudet, S Johnson, et al.
Human Molecular Genetics|May 1, 1993
Dinucleotide repeat polymorphism close to IDS gene in Xq27.3-q28 (DXS1113)C Weber, C Oudet, S Johnson, et al.
Human Genetics|June 1, 1997
A second family with XLRH displays the mutation S244L in the CLCN5 geneC Oudet, D Martin-Coignard, S Pannetier, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Strong founder effect for the fragile X syndrome in SwedenH Malmgren, K H Gustavson, C Oudet, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Striking founder effect for the fragile X syndrome in FinlandC Oudet, H von Koskull, A M Nordström, et al.
Journal of Medical Genetics|April 1, 1993
Characterisation of a highly polymorphic microsatellite at the DXS207 locus: confirmation of very close linkage to the retinoschisis disease geneC Oudet, C Weber, J Kaplan, et al.
Nature Genetics|June 1, 1994
FRAXAC2 instabilityR I Richards, K Holman, K Friend, et al.
American Journal of Human Genetics|May 1, 1992
Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2V Biancalana, M L Briard, A David, et al.
American Journal of Human Genetics|February 1, 1993
Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomesC Oudet, E Mornet, J L Serre, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Human Molecular Genetics|November 1, 1992
Two hot spots of recombination in the DMD gene correlate with the deletion prone regionsC Oudet, A Hanauer, P Clemens, et al.
Human Molecular Genetics|May 1, 1993
Dinucleotide repeat polymorphism at Xq26.1 (DXS1114)C Weber, C Oudet, S Johnson, et al.
Human Molecular Genetics|May 1, 1993
Dinucleotide repeat polymorphism close to IDS gene in Xq27.3-q28 (DXS1113)C Weber, C Oudet, S Johnson, et al.
Human Genetics|June 1, 1997
A second family with XLRH displays the mutation S244L in the CLCN5 geneC Oudet, D Martin-Coignard, S Pannetier, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Strong founder effect for the fragile X syndrome in SwedenH Malmgren, K H Gustavson, C Oudet, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Striking founder effect for the fragile X syndrome in FinlandC Oudet, H von Koskull, A M Nordström, et al.
Journal of Medical Genetics|April 1, 1993
Characterisation of a highly polymorphic microsatellite at the DXS207 locus: confirmation of very close linkage to the retinoschisis disease geneC Oudet, C Weber, J Kaplan, et al.
Nature Genetics|June 1, 1994
FRAXAC2 instabilityR I Richards, K Holman, K Friend, et al.
American Journal of Human Genetics|May 1, 1992
Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2V Biancalana, M L Briard, A David, et al.
American Journal of Human Genetics|February 1, 1993
Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomesC Oudet, E Mornet, J L Serre, et al.
Pageof 4