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A M Lossi

Showing results (1-10 of 17) with videos related to

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FEBS Letters|October 9, 1989
The mRNA transcripts from a mutant beta-globin gene derived from splicing at preferential cryptic sitesA M Lossi, J L Bergé-Lefranc
Journal of Medical Genetics|June 19, 2002
Mutation screening of the PKD1 transcript by RT-PCRS Burtey, A M Lossi, J Bayle, et al.
Gene|July 23, 1999
Transcript map of the human chromosome Xq11-Xq21 region: localization of 33 novel genes and one pseudogeneL Villard, J Belougne, A M Lossi, et al.
Hemoglobin|January 1, 1989
A further case of beta-thalassemia with an homozygous T----C substitution at the donor splice site of the first intervening sequence of the beta-globin geneA M Lossi, M Milland, J L Bergé-Lefranc, et al.
Human Molecular Genetics|September 1, 1993
Physical and transcriptional mapping of DXS56-PGK1 1 Mb region: identification of three new transcriptsJ Gecz, L Villard, A M Lossi, et al.
American Journal of Human Genetics|March 1, 1996
Splicing mutation in the ATR-X gene can lead to a dysmorphic mental retardation phenotype without alpha-thalassemiaL Villard, A Toutain, A M Lossi, et al.
Human Mutation|October 26, 1999
A polymorphic microsatellite XNP-GT in the XNP/ATRX gene's promotor allows familial indirect diagnosisN Lévy, R Bernard-Bronsard, A M Lossi, et al.
Genomics|July 15, 1997
Determination of the genomic structure of the XNP/ATRX gene encoding a potential zinc finger helicaseL Villard, A M Lossi, C Cardoso, et al.
American Journal of Human Genetics|July 27, 1999
Mutation of the XNP/ATR-X gene in a family with severe mental retardation, spastic paraplegia and skewed pattern of X inactivation: demonstration that the mutation is involved in the inactivation biasA M Lossi, J M Millán, L Villard, et al.
Journal of Medical Genetics|June 17, 2003
Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasiaN Philip, B Chabrol, A-M Lossi, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
FEBS Letters|October 9, 1989
The mRNA transcripts from a mutant beta-globin gene derived from splicing at preferential cryptic sitesA M Lossi, J L Bergé-Lefranc
Journal of Medical Genetics|June 19, 2002
Mutation screening of the PKD1 transcript by RT-PCRS Burtey, A M Lossi, J Bayle, et al.
Gene|July 23, 1999
Transcript map of the human chromosome Xq11-Xq21 region: localization of 33 novel genes and one pseudogeneL Villard, J Belougne, A M Lossi, et al.
Hemoglobin|January 1, 1989
A further case of beta-thalassemia with an homozygous T----C substitution at the donor splice site of the first intervening sequence of the beta-globin geneA M Lossi, M Milland, J L Bergé-Lefranc, et al.
Human Molecular Genetics|September 1, 1993
Physical and transcriptional mapping of DXS56-PGK1 1 Mb region: identification of three new transcriptsJ Gecz, L Villard, A M Lossi, et al.
American Journal of Human Genetics|March 1, 1996
Splicing mutation in the ATR-X gene can lead to a dysmorphic mental retardation phenotype without alpha-thalassemiaL Villard, A Toutain, A M Lossi, et al.
Human Mutation|October 26, 1999
A polymorphic microsatellite XNP-GT in the XNP/ATRX gene's promotor allows familial indirect diagnosisN Lévy, R Bernard-Bronsard, A M Lossi, et al.
Genomics|July 15, 1997
Determination of the genomic structure of the XNP/ATRX gene encoding a potential zinc finger helicaseL Villard, A M Lossi, C Cardoso, et al.
American Journal of Human Genetics|July 27, 1999
Mutation of the XNP/ATR-X gene in a family with severe mental retardation, spastic paraplegia and skewed pattern of X inactivation: demonstration that the mutation is involved in the inactivation biasA M Lossi, J M Millán, L Villard, et al.
Journal of Medical Genetics|June 17, 2003
Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasiaN Philip, B Chabrol, A-M Lossi, et al.
Pageof 2