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Cancer Genetics and Cytogenetics|May 1, 1987
Trisomy 4: another specific anomaly in acute nonlymphocytic leukemiaF Prieto, L Badía, M A Orts, et al.Cancer Genetics and Cytogenetics|October 1, 1987
Refractory anemia with monosomy 2 and a double minute chromosomeF Prieto, L Badía, F Gomis, et al.Anales Espanoles De Pediatria|March 1, 1976
[Chromosome delection point in "cri du chat" syndrome (author's transl)]F Prieto García, L Badía Garrabou, G Abeledo Mezquita, et al.Clinical Genetics|July 1, 1992
A fragile X family with high penetrance in females: risk heterogeneity?F Martínez, L Badía, F PrietoCancer Genetics and Cytogenetics|May 1, 1985
Translocation (11;22) in Ewing's sarcomaF Prieto, L Badía, J Montalar, et al.Cancer Genetics and Cytogenetics|April 1, 1988
Trisomy of the long arm of chromosome 1 in patients with hematologic malignancies and solid tumors: report of six casesF Cervantes, F Prieto, L Badía, et al.Cancer Genetics and Cytogenetics|January 1, 1993
Translocation (12;14)(q13;q32) in myelodysplastic syndromeL Badía, M A Alvarez, F Palau, et al.Anales Espanoles De Pediatria|December 1, 1977
[Translocation t (13:21) (q22:q22) in mother and monosomia 21 and partial trisomy 13 on her son (author's transl)]F Prieto García, L Badía Garrabou, J Ferrer CalvetteCancer Genetics and Cytogenetics|September 1, 1983
Translocation (15;17) in a child with variant form of acute promyelocytic leukemiaF Prieto, L Badia, V Castel, et al.Clinical Genetics|November 1, 1987
X-linked dysmorphic syndrome with mental retardationF Prieto, L Badía, F Mulas, et al.Pageof 13