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Showing results (71-80 of 78) with videos related to

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Nature Genetics|April 1, 1994
A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12D Bonnet, A Pelet, L Legeai-Mallet, et al.
Human Genetics|May 1, 1994
Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughterF Tihy, N Vogt, D Recan, et al.
American Journal of Human Genetics|February 1, 1995
A novel microsatellite DNA marker at locus D7S1870 detects hemizygosity in 75% of patients with Williams syndromeB Gilbert-Dussardier, D Bonneau, N Gigarel, et al.
American Journal of Human Genetics|February 1, 1994
A somatic origin of homologous Robertsonian translocations and isochromosomesW P Robinson, F Bernasconi, S Basaran, et al.
Human Molecular Genetics|April 1, 1994
Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus familyP Coucke, L Vits, G Van Camp, et al.
Genomics|October 1, 1992
The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52S Lyonnet, A Pelet, G Royer, et al.
Human Genetics|August 1, 1996
X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 geneC Ressot, P Latour, F Blanquet-Grossard, et al.
Annales De Genetique|January 1, 1997
Collaborative study of mosaic tetrasomy 12p or Pallister-Killian syndrome (nineteen fetuses or children)M Mathieu, C Piussan, F Thepot, et al.
Pageof 8

Showing results (71-80 of 78) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 78 results.
Nature Genetics|April 1, 1994
A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12D Bonnet, A Pelet, L Legeai-Mallet, et al.
Human Genetics|May 1, 1994
Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughterF Tihy, N Vogt, D Recan, et al.
American Journal of Human Genetics|February 1, 1995
A novel microsatellite DNA marker at locus D7S1870 detects hemizygosity in 75% of patients with Williams syndromeB Gilbert-Dussardier, D Bonneau, N Gigarel, et al.
American Journal of Human Genetics|February 1, 1994
A somatic origin of homologous Robertsonian translocations and isochromosomesW P Robinson, F Bernasconi, S Basaran, et al.
Human Molecular Genetics|April 1, 1994
Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus familyP Coucke, L Vits, G Van Camp, et al.
Genomics|October 1, 1992
The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52S Lyonnet, A Pelet, G Royer, et al.
Human Genetics|August 1, 1996
X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 geneC Ressot, P Latour, F Blanquet-Grossard, et al.
Annales De Genetique|January 1, 1997
Collaborative study of mosaic tetrasomy 12p or Pallister-Killian syndrome (nineteen fetuses or children)M Mathieu, C Piussan, F Thepot, et al.
Pageof 8