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E Vamos

Showing results (91-100 of 129) with videos related to

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Bulletins Et Memoires De La Societe Francaise D'Ophtalmologie|January 1, 1977
[Mannosidosis: diagnosis by conjunctival biopsy and enzymatic analysis of the tears]J Libert, F Van Hoof, J P Farriaux, et al.
Research in Immunology|November 1, 1991
Analysis of the peripheral T-cell compartment in the MHC class II deficiency syndromeM Lambert, M van Eggermond, M Andrien, et al.
Medical and Pediatric Oncology|January 1, 1994
Anaplastic large cell lymphoma of true histiocytic origin in an infant: unusual clinical, hematological, and cytogenetic featuresA Ferster, F Corazza, P Heimann, et al.
Acta Paediatrica Belgica|April 1, 1976
Antenatal diagnosis of congenital diseases through cultured amniotic cells: results of 149 amniocentesesE Vamos-Hurwitz, P Petit, I Liebaers, et al.
American Journal of Medical Genetics|March 1, 1986
Lethal osteopetrosis with multiple fractures in uteroN el Khazen, D Faverly, E Vamos, et al.
Cancer Genetics and Cytogenetics|December 1, 1995
Multiple clonal chromosome aberrations in a case of childhood focal nodular hyperplasia of the liverP Heimann, G Ogur, C Debusscher, et al.
Revue Medicale De Bruxelles|June 1, 1992
[Bone marrow graft in hereditary diseases]W Bujan, A Ferster, C Devalck, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
Neonatal multiple sulphatase deficiency disorder: biochemical characterizationY Eto, T Tokoro, Y Kureha, et al.
Journal of Medical Genetics|October 1, 1983
C heterochromatin variation in couples with recurrent early abortionsA Maes, C Staessen, L Hens, et al.
The Journal of Pediatrics|March 1, 1984
Congenital malformations in 10,000 consecutive births in a university hospital: need for genetic counseling and prenatal diagnosisN Van Regemorter, J Dodion, C Druart, et al.
Pageof 13

Showing results (91-100 of 129) with videos related to

Sort By:
Pageof 13
Bulletins Et Memoires De La Societe Francaise D'Ophtalmologie|January 1, 1977
[Mannosidosis: diagnosis by conjunctival biopsy and enzymatic analysis of the tears]J Libert, F Van Hoof, J P Farriaux, et al.
Research in Immunology|November 1, 1991
Analysis of the peripheral T-cell compartment in the MHC class II deficiency syndromeM Lambert, M van Eggermond, M Andrien, et al.
Medical and Pediatric Oncology|January 1, 1994
Anaplastic large cell lymphoma of true histiocytic origin in an infant: unusual clinical, hematological, and cytogenetic featuresA Ferster, F Corazza, P Heimann, et al.
Acta Paediatrica Belgica|April 1, 1976
Antenatal diagnosis of congenital diseases through cultured amniotic cells: results of 149 amniocentesesE Vamos-Hurwitz, P Petit, I Liebaers, et al.
American Journal of Medical Genetics|March 1, 1986
Lethal osteopetrosis with multiple fractures in uteroN el Khazen, D Faverly, E Vamos, et al.
Cancer Genetics and Cytogenetics|December 1, 1995
Multiple clonal chromosome aberrations in a case of childhood focal nodular hyperplasia of the liverP Heimann, G Ogur, C Debusscher, et al.
Revue Medicale De Bruxelles|June 1, 1992
[Bone marrow graft in hereditary diseases]W Bujan, A Ferster, C Devalck, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
Neonatal multiple sulphatase deficiency disorder: biochemical characterizationY Eto, T Tokoro, Y Kureha, et al.
Journal of Medical Genetics|October 1, 1983
C heterochromatin variation in couples with recurrent early abortionsA Maes, C Staessen, L Hens, et al.
The Journal of Pediatrics|March 1, 1984
Congenital malformations in 10,000 consecutive births in a university hospital: need for genetic counseling and prenatal diagnosisN Van Regemorter, J Dodion, C Druart, et al.
Pageof 13