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C Junien

Showing results (151-160 of 284) with videos related to

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Nouvelle Revue Francaise D'Hematologie|May 1, 1972
[Biochemical study of a case of erythroleukemia. Demonstration in an abnormal erythrocyte population of simultaneous anomalies of hemoglobin and glycolysis enzymes]J Pagnier, D Labie, J C Kaplan, et al.
Revue Des Maladies Respiratoires|January 1, 1991
[Tracheo-bronchial granular cell tumors. Apropos of 4 cases]F Blanc-Jouvan, E Brambilla, A Bosseray, et al.
The Journal of Clinical Investigation|January 1, 1991
Anderson's disease: genetic exclusion of the apolipoprotein-B gene in two familiesM Pessah, P Benlian, I Beucler, et al.
Human Genetics|January 1, 1981
Retinoblastoma-del(13q14): report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase DH Rivera, C Turleau, J de Grouchy, et al.
Nucleic Acids Research|January 1, 1997
Software and database for the analysis of mutations in the human LDL receptor geneM Varret, J P Rabès, G Collod-Béroud, et al.
Genomics|December 1, 1990
Direct haplotyping by double digestion of PCR-amplified creatine kinase (CKMM): application to myotonic dystrophy diagnosisC Lavedan, C Duros, D Savoy, et al.
Bulletin Du Cancer|January 1, 1991
[Antioncogenes: models for tumors in children]C Junien, I Henry, C Jeanpierre, et al.
Journal of Medical Genetics|February 1, 1991
Prenatal diagnosis of myotonic dystrophy using closely linked flanking markersC Lavedan, H Hofmann, P Shelbourne, et al.
Annales De Genetique|June 1, 1975
Partial deletion of the short arm of chromosome 12(p11; p13). Report of a caseR Tenconi, C Baccichetti, F Anglani, et al.
Journal of Medical Genetics|May 16, 2002
Major difference in aetiology and phenotypic abnormalities between transient and permanent neonatal diabetesE Marquis, J J Robert, C Bouvattier, et al.
Pageof 29

Showing results (151-160 of 284) with videos related to

Sort By:
Pageof 29
Nouvelle Revue Francaise D'Hematologie|May 1, 1972
[Biochemical study of a case of erythroleukemia. Demonstration in an abnormal erythrocyte population of simultaneous anomalies of hemoglobin and glycolysis enzymes]J Pagnier, D Labie, J C Kaplan, et al.
Revue Des Maladies Respiratoires|January 1, 1991
[Tracheo-bronchial granular cell tumors. Apropos of 4 cases]F Blanc-Jouvan, E Brambilla, A Bosseray, et al.
The Journal of Clinical Investigation|January 1, 1991
Anderson's disease: genetic exclusion of the apolipoprotein-B gene in two familiesM Pessah, P Benlian, I Beucler, et al.
Human Genetics|January 1, 1981
Retinoblastoma-del(13q14): report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase DH Rivera, C Turleau, J de Grouchy, et al.
Nucleic Acids Research|January 1, 1997
Software and database for the analysis of mutations in the human LDL receptor geneM Varret, J P Rabès, G Collod-Béroud, et al.
Genomics|December 1, 1990
Direct haplotyping by double digestion of PCR-amplified creatine kinase (CKMM): application to myotonic dystrophy diagnosisC Lavedan, C Duros, D Savoy, et al.
Bulletin Du Cancer|January 1, 1991
[Antioncogenes: models for tumors in children]C Junien, I Henry, C Jeanpierre, et al.
Journal of Medical Genetics|February 1, 1991
Prenatal diagnosis of myotonic dystrophy using closely linked flanking markersC Lavedan, H Hofmann, P Shelbourne, et al.
Annales De Genetique|June 1, 1975
Partial deletion of the short arm of chromosome 12(p11; p13). Report of a caseR Tenconi, C Baccichetti, F Anglani, et al.
Journal of Medical Genetics|May 16, 2002
Major difference in aetiology and phenotypic abnormalities between transient and permanent neonatal diabetesE Marquis, J J Robert, C Bouvattier, et al.
Pageof 29