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Hormone Research|January 1, 1997
A case with 47,XXY,del(15)(q11;q13) karyotype associated with Prader-Willi phenotypeA Rego, M D Coll, M Regal, et al.
Bone Marrow Transplantation|August 6, 1999
Follow-up of chimerism in children with hematological diseases after allogeneic hematopoietic progenitor cell transplantsM Ortega, T Escudero, M R Caballín, et al.
Cancer Genetics and Cytogenetics|July 1, 1991
Isochromosome 14q in myeloid dysplastic disorderF Solé, M R Caballín, M D Coll, et al.
Cancer Genetics and Cytogenetics|June 1, 1992
New chromosomal abnormality. t(1;19;?) in a case of B-chronic lymphocytic leukemiaS Montero, M R Caballín, M D Coll, et al.
Revista De Neurologia|March 1, 2006
[From the clinical to the genetic diagnosis of Prader-Willi and Angelman syndromes]C Camprubí-Sánchez, E Gabau-Vila, J Artigas-Pallarés, et al.
Cancer Genetics and Cytogenetics|June 1, 1992
Cytogenetic studies in acute nonlymphocytic leukemiaF Solé, M R Caballín, M D Coll, et al.
Cancer Genetics and Cytogenetics|February 1, 1990
Cytogenetic study of a patient with the Sézary syndromeF Solé, N Tarrida, M D Coll, et al.
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