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  1.  

    Performance characteristics of GaN/Al~0~, ~2Ga~0~, ~8N quantum dot laser at L = 100 Å

    Bouchenafa, H. / Benichou, B. / Bouabdallah, B. | British Library Online Contents | 2019
  2.  

    Improved resolution method to study at 3D the conduction phenomena inside GaAs PIN photodiode

    Bouabdallah, B. / Bourezig, Y. / Benichou, B. | Tema Archive | 2010
  3.  

    Improved resolution method to study at 3D the conduction phenomena inside GaAs PIN photodiode

    Bouabdallah, B. / Bourezig, Y. / Benichou, B. | British Library Online Contents | 2010
  4.  

    Design and characteristics of blue Nitride multi-quantum well and SCH-SQW Lasers

    Bouabdallah, B. / Benichou, B. / Menezla, R. et al. | British Library Online Contents | 2007
  5.  

    Sparsity vs. statistical independence from a best-basis viewpoint (Invited Paper) [4119-54]

    Saito, N. / Larson, B. M. / Benichou, B. et al. | British Library Conference Proceedings | 2000
  6.  

    Sparsity vs. statistical independence from a best-basis viewpoint (Invited Paper) [4119-54]

    Saito, N. / Larson, B. M. / Benichou, B. et al. | British Library Conference Proceedings | 2000
  7.  

    Further Evidence for Genetic Heterogeneity Within Type II Autosomal Dominant Osteopetrosis

    Bénichou, O. D. / Bénichou, B. / Copin, H. et al. | Wiley | 2000
  8.  

    Effective clearance of GL-3 in a human iPSC-derived cardiomyocyte model of Fabry disease

    Itier, J. M. / Ret, G. n. / Viale, S. et al. | British Library Online Contents | 2014
  9.  

    Rapid Diagnostic Test for Detection of Cys28Tyr Mutation in Hereditary Hemochromatosis

    Andre, M.-T. / Jacquemont, S. / Renault, S. et al. | British Library Online Contents | 1998
  10.  

    Evidence for Genetic Heterogeneity in Albers Schonberg Osteopetrosis

    Benichou, O. D. / Benichou, B. / Le Merrer, M. et al. | British Library Conference Proceedings | 1998
  11.  

    De novo and inherited deletions of the 5q13 region in spinal muscular atrophies

    National licence
    Melki, J / Lefebvre, S / Burglen, L et al. | AAAS | 1994
  12.  

    De Novo and Inherited Deletions of the 5q13 Region in Spinal Muscular Atrophies

    Melki, J. / Lefebvre, S. / Burglen, L. et al. | Online Contents | 1994
  13.  

    Identification and Characterization of a Spinal Muscular Atrophy-Determining Gene

    Lefebvre, S. / Bürglen, L. / Reboullet, S. et al. | Online Contents | 1995
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