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M Deminatti

Showing results (51-60 of 77) with videos related to

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Annales De Genetique|January 1, 1989
Cytogenetic studies in 30 patients with Burkitt's lymphoma or L3 acute lymphoblastic leukemia with special reference to additional chromosome abnormalitiesJ L Lai, P Fenaux, M Zandecki, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1983
[Subacute pre-eclampsia and hydramnios as manifestation of fetal triploidy. In utero diagnosis in the 28th week]C Dognin, J C Monnier, B Lanciaux, et al.
Cancer Genetics and Cytogenetics|October 15, 1989
A new case of dic(9;12)(p13;p11) in acute lymphocytic leukemiaJ L Lai, M Deminatti, M H Estienne, et al.
Annales De Genetique|January 1, 1988
Usefulness of linked DNA probes for prenatal diagnosis of cystic fibrosis: report of a case in a 1:4 risk pregnancyF Fontaine, F Vasseur, J B Savary, et al.
Cancer Genetics and Cytogenetics|March 1, 1987
Chronic myelogenous leukemia with t(9;22) and t(8;11): a new chromosome anomalyJ L Laï, J P Jouet, J B Savary, et al.
Archives Francaises De Pediatrie|April 1, 1971
[The cardiopathies of Ullrich-Turner syndrome]C Dupuis, M Deminatti, E Maillard, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1983
[Burkitt's acute lymphoblastic leukemia. Incidence and cytogenetic aspects]J L Laï, J P Jouet, M Zandecki, et al.
Hematological Oncology|July 1, 1989
Cytogenetics and their prognostic value in childhood and adult acute lymphoblastic leukemia (ALL) excluding L3P Fenaux, J L Lai, P Morel, et al.
Cancer Genetics and Cytogenetics|June 1, 1990
Translocations (5;17) and (7;17) in patients with de novo or therapy-related myelodysplastic syndromes or acute nonlymphocytic leukemia. A possible association with acquired pseudo-Pelger-Huët anomaly and small vacuolated granulocytesJ L Laï, M Zandecki, P Fenaux, et al.
Lille Medical : Journal De La Faculte De Medecine Et De Pharmacie De L'Universite De Lille|December 1, 1979
[Men with karyotype 46, XX (apropos of 2 cases)]P Fossati, J B Savary, J J Boutemy, et al.
Pageof 8

Showing results (51-60 of 77) with videos related to

Sort By:
Pageof 8
Annales De Genetique|January 1, 1989
Cytogenetic studies in 30 patients with Burkitt's lymphoma or L3 acute lymphoblastic leukemia with special reference to additional chromosome abnormalitiesJ L Lai, P Fenaux, M Zandecki, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1983
[Subacute pre-eclampsia and hydramnios as manifestation of fetal triploidy. In utero diagnosis in the 28th week]C Dognin, J C Monnier, B Lanciaux, et al.
Cancer Genetics and Cytogenetics|October 15, 1989
A new case of dic(9;12)(p13;p11) in acute lymphocytic leukemiaJ L Lai, M Deminatti, M H Estienne, et al.
Annales De Genetique|January 1, 1988
Usefulness of linked DNA probes for prenatal diagnosis of cystic fibrosis: report of a case in a 1:4 risk pregnancyF Fontaine, F Vasseur, J B Savary, et al.
Cancer Genetics and Cytogenetics|March 1, 1987
Chronic myelogenous leukemia with t(9;22) and t(8;11): a new chromosome anomalyJ L Laï, J P Jouet, J B Savary, et al.
Archives Francaises De Pediatrie|April 1, 1971
[The cardiopathies of Ullrich-Turner syndrome]C Dupuis, M Deminatti, E Maillard, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1983
[Burkitt's acute lymphoblastic leukemia. Incidence and cytogenetic aspects]J L Laï, J P Jouet, M Zandecki, et al.
Hematological Oncology|July 1, 1989
Cytogenetics and their prognostic value in childhood and adult acute lymphoblastic leukemia (ALL) excluding L3P Fenaux, J L Lai, P Morel, et al.
Cancer Genetics and Cytogenetics|June 1, 1990
Translocations (5;17) and (7;17) in patients with de novo or therapy-related myelodysplastic syndromes or acute nonlymphocytic leukemia. A possible association with acquired pseudo-Pelger-Huët anomaly and small vacuolated granulocytesJ L Laï, M Zandecki, P Fenaux, et al.
Lille Medical : Journal De La Faculte De Medecine Et De Pharmacie De L'Universite De Lille|December 1, 1979
[Men with karyotype 46, XX (apropos of 2 cases)]P Fossati, J B Savary, J J Boutemy, et al.
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