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M Claustres

Showing results (31-40 of 143) with videos related to

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European Journal of Pediatrics|October 1, 1986
A paediatric case of sideroblastic anaemia. Ultrastructural studies of erythroblasts cultured from marrow BFU-E in a methylcellulose micromethodM Claustres, H Vannereau, H Bellet, et al.
Ophthalmic Genetics|November 15, 1997
A complex allele (1064delTC and IVS2 + 22ins7) in the peripherin/RDS gene in retinitis pigmentosa with macular dystrophyC Bareil, C Hamel, B Arnaud, et al.
Journal of Medical Genetics|January 1, 1994
Severe pulmonary and digestive disease in a cystic fibrosis child homozygous for G542XM Desgeorges, M Laussel, B Rollin, et al.
Human Genetics|December 1, 1993
Rapid detection of single nucleotide deletions: application to the beta 6 (-A) mutation of the beta-globin gene and to cystic fibrosisM C Romey, P Aguilar-Martinez, J Demaille, et al.
Journal Francais D'Ophtalmologie|October 6, 1998
[Retinoblastoma: importance of genetic counseling]A Girardet, L Beaufrere, S Tuffery, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Becker muscular dystrophy: demonstration of the carrier status of a female by immunoblotting and immunostainingM P Chevron, S Tuffery, B Echenne, et al.
Human Mutation|June 22, 2000
W179R: a novel missense mutation in the peripherin/RDS gene in a family with autosomal dominant retinitis pigmentosaC Bareil, V Delague, B Arnaud, et al.
Revue Neurologique|October 20, 2009
[Monogenetic dystonia: revisiting the dopaminergic hypothesis]A Blanchard, A Roubertie, M Y Frédéric, et al.
Pathologie-Biologie|December 1, 1982
Study of human isoferritins from liver, spleen, heart and placenta by the microcomplement fixation techniqueM Claustres, F Guilleux, V Sieso, et al.
Journal of Assisted Reproduction and Genetics|March 1, 1997
Amplification of the RB1.20 polymorphism in single spermatozoaA Girardet, F Pellestor, S Tuffery, et al.
Pageof 15

Showing results (31-40 of 143) with videos related to

Sort By:
Pageof 15
European Journal of Pediatrics|October 1, 1986
A paediatric case of sideroblastic anaemia. Ultrastructural studies of erythroblasts cultured from marrow BFU-E in a methylcellulose micromethodM Claustres, H Vannereau, H Bellet, et al.
Ophthalmic Genetics|November 15, 1997
A complex allele (1064delTC and IVS2 + 22ins7) in the peripherin/RDS gene in retinitis pigmentosa with macular dystrophyC Bareil, C Hamel, B Arnaud, et al.
Journal of Medical Genetics|January 1, 1994
Severe pulmonary and digestive disease in a cystic fibrosis child homozygous for G542XM Desgeorges, M Laussel, B Rollin, et al.
Human Genetics|December 1, 1993
Rapid detection of single nucleotide deletions: application to the beta 6 (-A) mutation of the beta-globin gene and to cystic fibrosisM C Romey, P Aguilar-Martinez, J Demaille, et al.
Journal Francais D'Ophtalmologie|October 6, 1998
[Retinoblastoma: importance of genetic counseling]A Girardet, L Beaufrere, S Tuffery, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Becker muscular dystrophy: demonstration of the carrier status of a female by immunoblotting and immunostainingM P Chevron, S Tuffery, B Echenne, et al.
Human Mutation|June 22, 2000
W179R: a novel missense mutation in the peripherin/RDS gene in a family with autosomal dominant retinitis pigmentosaC Bareil, V Delague, B Arnaud, et al.
Revue Neurologique|October 20, 2009
[Monogenetic dystonia: revisiting the dopaminergic hypothesis]A Blanchard, A Roubertie, M Y Frédéric, et al.
Pathologie-Biologie|December 1, 1982
Study of human isoferritins from liver, spleen, heart and placenta by the microcomplement fixation techniqueM Claustres, F Guilleux, V Sieso, et al.
Journal of Assisted Reproduction and Genetics|March 1, 1997
Amplification of the RB1.20 polymorphism in single spermatozoaA Girardet, F Pellestor, S Tuffery, et al.
Pageof 15