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M Desgeorges

Showing results (51-60 of 84) with videos related to

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Human Molecular Genetics|April 1, 1994
Homozygosity for a novel missense mutation (I175V) in exon 5 of the CFTR gene in a family of Armenian descentM C Romey, M Desgeorges, P Malzac, et al.
Human Mutation|January 1, 1995
Novel missense mutation in the first transmembrane segment of the CFTR gene (Q98R) identified in a male adultM C Romey, M Desgeorges, P Ray, et al.
Neuro-Chirurgie|June 16, 2000
[Neuronavigation in third ventricle tumors]R Dulou, F De Soultrait, E Blondet, et al.
Neuro-Chirurgie|December 17, 2002
[Contribution of perfusion magnetic resonance imaging in a patient with cerebral ganglioglioma]P Métellus, A Ait Ameur, T Faillot, et al.
Human Genetics|September 1, 1996
Transcript analysis of CFTR frameshift mutations in lymphocytes using the reverse transcription-polymerase chain reaction technique and the protein truncation testM C Romey, S Tuffery, M Desgeorges, et al.
Human Genetics|August 1, 1997
Cystic fibrosis in Lebanon: distribution of CFTR mutations among Arab communitiesM Desgeorges, A Mégarbané, C Guittard, et al.
Prenatal Diagnosis|February 1, 1993
Prenatal diagnosis for cystic fibrosis using SSCP analysisM Desgeorges, P Boulot, P Kjellberg, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|December 1, 1996
[Toxic aluminum encephalopathy. Predominant involvement of the limbic system on MRI]C Lévêque, D Soulié, J L Sarrazin, et al.
Human Molecular Genetics|June 1, 1994
Two novel rare frameshift mutations (2423 del G in exon 13 and 1215 del G in exon 7) and one novel rare sequence variation (3271 + 18 C or T) identified in a patient with cystic fibrosisM C Romey, M Desgeorges, M Laussel, et al.
Clinical Genetics|February 13, 2001
The molecular basis of cystic fibrosis in South AfricaA Goldman, R Labrum, M Claustres, et al.
Pageof 9

Showing results (51-60 of 84) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|April 1, 1994
Homozygosity for a novel missense mutation (I175V) in exon 5 of the CFTR gene in a family of Armenian descentM C Romey, M Desgeorges, P Malzac, et al.
Human Mutation|January 1, 1995
Novel missense mutation in the first transmembrane segment of the CFTR gene (Q98R) identified in a male adultM C Romey, M Desgeorges, P Ray, et al.
Neuro-Chirurgie|June 16, 2000
[Neuronavigation in third ventricle tumors]R Dulou, F De Soultrait, E Blondet, et al.
Neuro-Chirurgie|December 17, 2002
[Contribution of perfusion magnetic resonance imaging in a patient with cerebral ganglioglioma]P Métellus, A Ait Ameur, T Faillot, et al.
Human Genetics|September 1, 1996
Transcript analysis of CFTR frameshift mutations in lymphocytes using the reverse transcription-polymerase chain reaction technique and the protein truncation testM C Romey, S Tuffery, M Desgeorges, et al.
Human Genetics|August 1, 1997
Cystic fibrosis in Lebanon: distribution of CFTR mutations among Arab communitiesM Desgeorges, A Mégarbané, C Guittard, et al.
Prenatal Diagnosis|February 1, 1993
Prenatal diagnosis for cystic fibrosis using SSCP analysisM Desgeorges, P Boulot, P Kjellberg, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|December 1, 1996
[Toxic aluminum encephalopathy. Predominant involvement of the limbic system on MRI]C Lévêque, D Soulié, J L Sarrazin, et al.
Human Molecular Genetics|June 1, 1994
Two novel rare frameshift mutations (2423 del G in exon 13 and 1215 del G in exon 7) and one novel rare sequence variation (3271 + 18 C or T) identified in a patient with cystic fibrosisM C Romey, M Desgeorges, M Laussel, et al.
Clinical Genetics|February 13, 2001
The molecular basis of cystic fibrosis in South AfricaA Goldman, R Labrum, M Claustres, et al.
Pageof 9