Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M D Coll

Showing results (11-20 of 26) with videos related to

Pageof 3
Sort By:
Cancer Genetics and Cytogenetics|October 1, 1990
Acute lymphoblastic leukemia with t(4;11) in a patient previously exposed to a carcinogenF Solé, M R Caballín, M D Coll, et al.
British Journal of Haematology|November 25, 2000
Follow-up by cytogenetic and fluorescence in situ hybridization analysis of allogeneic bone marrow transplantation in two children with Fanconi's anaemia in transformationM Ortega, M R Caballín, J J Ortega, et al.
American Journal of Medical Genetics|December 22, 1999
SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphroditeE Margarit, M D Coll, R Oliva, et al.
Cancer Genetics and Cytogenetics|January 29, 2003
AML1 amplification in a child with acute lymphoblastic leukemiaYolanda Alvarez, M D Coll, P Bastida, et al.
Cancer Genetics and Cytogenetics|March 1, 1995
Isochromosome 14q in childhood acute lymphoblastic leukemiaL Tusell, M R Caballín, M D Coll, et al.
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.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Cancer Genetics and Cytogenetics|October 1, 1990
Acute lymphoblastic leukemia with t(4;11) in a patient previously exposed to a carcinogenF Solé, M R Caballín, M D Coll, et al.
British Journal of Haematology|November 25, 2000
Follow-up by cytogenetic and fluorescence in situ hybridization analysis of allogeneic bone marrow transplantation in two children with Fanconi's anaemia in transformationM Ortega, M R Caballín, J J Ortega, et al.
American Journal of Medical Genetics|December 22, 1999
SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphroditeE Margarit, M D Coll, R Oliva, et al.
Cancer Genetics and Cytogenetics|January 29, 2003
AML1 amplification in a child with acute lymphoblastic leukemiaYolanda Alvarez, M D Coll, P Bastida, et al.
Cancer Genetics and Cytogenetics|March 1, 1995
Isochromosome 14q in childhood acute lymphoblastic leukemiaL Tusell, M R Caballín, M D Coll, et al.
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.
Pageof 3