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B Bénichou

Showing results (1-10 of 9) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|May 15, 1991
Class II-antigen-negative patient and mutant B-cell lines represent at least three, and probably four, distinct genetic defects defined by complementation analysisB Bénichou, J L Strominger
Revue Du Rhumatisme (English Ed.)|January 29, 1999
Osteopetrosis as a model for studying bone resorptionO D Bénichou, B Bénichou, M C de Vernejoul
Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
Study on possible increase in twinning rate at a small village in south BrazilU Matte, M G Le Roux, B Bénichou, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 12, 2000
Further evidence for genetic heterogeneity within type II autosomal dominant osteopetrosisO D Bénichou, B Bénichou, H Copin, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1991
Mutations in the D strand of the human CD4 V1 domain affect CD4 interactions with the human immunodeficiency virus envelope glycoprotein gp120 and HLA class II antigens similarlyD Piatier-Tonneau, L N Gastinel, G Moussy, et al.
Journal of the American College of Cardiology|June 7, 2000
Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28J N Trochu, F Kyndt, J J Schott, et al.
Science (New York, N.Y.)|June 3, 1994
De novo and inherited deletions of the 5q13 region in spinal muscular atrophiesJ Melki, S Lefebvre, L Burglen, et al.
Blood|April 15, 1996
Possible misdiagnosis of factor VIII gene inversion in a case of severe hemophilia AB Bénichou, O Herbert, S Huet, et al.
American Journal of Human Genetics|April 29, 1998
Mapping of X-linked myxomatous valvular dystrophy to chromosome Xq28F Kyndt, J J Schott, J N Trochu, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Proceedings of the National Academy of Sciences of the United States of America|May 15, 1991
Class II-antigen-negative patient and mutant B-cell lines represent at least three, and probably four, distinct genetic defects defined by complementation analysisB Bénichou, J L Strominger
Revue Du Rhumatisme (English Ed.)|January 29, 1999
Osteopetrosis as a model for studying bone resorptionO D Bénichou, B Bénichou, M C de Vernejoul
Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
Study on possible increase in twinning rate at a small village in south BrazilU Matte, M G Le Roux, B Bénichou, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 12, 2000
Further evidence for genetic heterogeneity within type II autosomal dominant osteopetrosisO D Bénichou, B Bénichou, H Copin, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1991
Mutations in the D strand of the human CD4 V1 domain affect CD4 interactions with the human immunodeficiency virus envelope glycoprotein gp120 and HLA class II antigens similarlyD Piatier-Tonneau, L N Gastinel, G Moussy, et al.
Journal of the American College of Cardiology|June 7, 2000
Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28J N Trochu, F Kyndt, J J Schott, et al.
Science (New York, N.Y.)|June 3, 1994
De novo and inherited deletions of the 5q13 region in spinal muscular atrophiesJ Melki, S Lefebvre, L Burglen, et al.
Blood|April 15, 1996
Possible misdiagnosis of factor VIII gene inversion in a case of severe hemophilia AB Bénichou, O Herbert, S Huet, et al.
American Journal of Human Genetics|April 29, 1998
Mapping of X-linked myxomatous valvular dystrophy to chromosome Xq28F Kyndt, J J Schott, J N Trochu, et al.
Pageof 1