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Anales Espanoles De Pediatria|January 1, 1982
[Holt-Oram syndrome with chromosomopathy (author's transl)]C González Espinosa, L Artiles Pérez, M García Báez, et al.American Journal of Medical Genetics|January 20, 1997
De novo trisomy 16pJ L Carrasco Juan, J C Cigudosa, A Otero Gómez, et al.Cancer Genetics and Cytogenetics|December 1, 1992
Deletion (7)(p11p15) in a patient with Philadelphia-positive chronic myelogenous leukemiaJ L Carrasco Juan, A Otero Gómez, J L García Miranda, et al.Journal of Medical Genetics|February 1, 1983
Monosomy 22 with humoral immunodeficiency: is there an immunoglobulin chain deficit?J L García Miranda, A Otero Gómez, H Varela Ansedes, et al.Cancer Genetics and Cytogenetics|July 15, 1992
AML with unusual chromosomal changes. Translocation (15;21) and 5q- in the presence of two normal chromosomes 5J L Carrasco Juan, A Otero Gómez, J L Garcia Miranda, et al.Cancer Genetics and Cytogenetics|October 1, 1996
Deletion of exon b3 of the BCR gene in CML: easy breakpoint mapping by a two-round PCRJ C Cigudosa, M T Acosta Almeida, J L Carrasco Juan, et al.British Journal of Haematology|December 1, 1995
BCR-ABL rearrangement and 'variant' Philadelphia chromosome in de novo acute myelogenous leukaemia FAB subtype M1J C Cigudosa, M T Acosta Almeida, V Carrasco, et al.Prenatal Diagnosis|June 1, 1989
A rare case of de novo structural rearrangement of X chromosome diagnosed by amniocentesisJ L Carrasco Juan, A Otero Gómez, M C Vilar Mesa, et al.Cancer Genetics and Cytogenetics|July 1, 1995
Translocation (5;19)(q13;q13) in a multinodular thyroid goiterJ C Cigudosa, A Pedrosa Guerra, A Otero Gómez, et al.Annales De Genetique|January 1, 1990
Small marker chromosomes in a series of 1,000 prenatal diagnoses by amniocentesisJ L Carrasco Juan, A Otero Gómez, M C Vilar Mesa, et al.Pageof 1