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F Prieto

Showing results (51-60 of 157) with videos related to

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Medicina Clinica|May 3, 2001
[Early diagnosis of retinoblastoma: usefulness of searching for RB1 gene mutations]C Nájera, F Sánchez, E Mateu, et al.
Cancer Genetics and Cytogenetics|December 1, 1982
Chromosome banding patterns in patients with chronic myelocytic leukemiaF Carbonell, J Benitez, F Prieto, et al.
Cancer Genetics and Cytogenetics|August 1, 1986
Cytogenetic studies in 18 patients with secondary blood disordersJ Benitez, F Carbonell, T Ferro, et al.
Sangre|January 1, 1978
[Trysomy of chromosome 1 long arms plus chromosome 9 inversion in leukaemic cells (author's transl)]F Prieto, L Badia, J Mayans, et al.
Medicina Clinica|May 6, 1995
[The diagnosis and prevalence of locus CMT1A duplication in Charcot-Marie-Tooth disease type 1]S Bort, T Sevilla, J J Vílchez, et al.
Prenatal Diagnosis|June 1, 1995
Prenatal diagnosis of Friedreich ataxia: improved accuracy by using new genetic flanking markersE Monros, P Smeyers, M A Ramos, et al.
Human Genetics|January 1, 1981
Pericentric inversions of chromosome 12 in two familiesF Prieto, L Badía, F Asensi, et al.
Sangre|January 1, 1978
[Twenty-six chromosomes hypodiploidy in acute lymphoblastic leukaemia (author's transl)]F Prieto, L Badia, J Mayans, et al.
Human Genetics|December 18, 1978
10p- syndrome associated with multiple chromosomal abnormalitiesF Prieto, L Badia, J A Moreno, et al.
Cancer Genetics and Cytogenetics|May 1, 1987
Trisomy 4: another specific anomaly in acute nonlymphocytic leukemiaF Prieto, L Badía, M A Orts, et al.
Pageof 16

Showing results (51-60 of 157) with videos related to

Sort By:
Pageof 16
Medicina Clinica|May 3, 2001
[Early diagnosis of retinoblastoma: usefulness of searching for RB1 gene mutations]C Nájera, F Sánchez, E Mateu, et al.
Cancer Genetics and Cytogenetics|December 1, 1982
Chromosome banding patterns in patients with chronic myelocytic leukemiaF Carbonell, J Benitez, F Prieto, et al.
Cancer Genetics and Cytogenetics|August 1, 1986
Cytogenetic studies in 18 patients with secondary blood disordersJ Benitez, F Carbonell, T Ferro, et al.
Sangre|January 1, 1978
[Trysomy of chromosome 1 long arms plus chromosome 9 inversion in leukaemic cells (author's transl)]F Prieto, L Badia, J Mayans, et al.
Medicina Clinica|May 6, 1995
[The diagnosis and prevalence of locus CMT1A duplication in Charcot-Marie-Tooth disease type 1]S Bort, T Sevilla, J J Vílchez, et al.
Prenatal Diagnosis|June 1, 1995
Prenatal diagnosis of Friedreich ataxia: improved accuracy by using new genetic flanking markersE Monros, P Smeyers, M A Ramos, et al.
Human Genetics|January 1, 1981
Pericentric inversions of chromosome 12 in two familiesF Prieto, L Badía, F Asensi, et al.
Sangre|January 1, 1978
[Twenty-six chromosomes hypodiploidy in acute lymphoblastic leukaemia (author's transl)]F Prieto, L Badia, J Mayans, et al.
Human Genetics|December 18, 1978
10p- syndrome associated with multiple chromosomal abnormalitiesF Prieto, L Badia, J A Moreno, et al.
Cancer Genetics and Cytogenetics|May 1, 1987
Trisomy 4: another specific anomaly in acute nonlymphocytic leukemiaF Prieto, L Badía, M A Orts, et al.
Pageof 16