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Haematologica|May 10, 2007
Molecular genetic analyses in familial and sporadic congenital primary erythrocytosisSusana Rives, Heike L Pahl, Lourdes Florensa, et al.
Leukemia Research|April 20, 2013
Genetic predisposition to molecular response in patients with myeloproliferative neoplasms treated with hydroxycarbamideAnna Angona, Beatriz Bellosillo, Alberto Alvarez-Larrán, et al.
British Journal of Haematology|July 22, 2014
The role of serum erythropoietin level and JAK2 V617F allele burden in the diagnosis of polycythaemia veraAgueda Ancochea, Alberto Alvarez-Larrán, Cristian Morales-Indiano, et al.
Histology and Histopathology|March 5, 2021
Diagnostic usefulness of immunohistochemical evaluation of CD1a antigen and polyclonal anti-leishmania antibodies in cutaneous leishmaniasisEmilio Lopez-Trujillo, Mònica Gonzàlez-Farré, Ramon M Pujol, et al.
Cancer Genetics and Cytogenetics|December 21, 2005
Study of chromosomal abnormalities in 11 cases of cervical dysplasia using comparative genomic hybridization on cotton-lint cervical samplesCarlota Costa, Pere Fuste, Francesc Alameda, et al.
Acta Dermato-Venereologica|April 23, 2005
Lymphomatoid papulosis associated with mycosis fungoides: clinicopathological and molecular studies of 12 casesFernando Gallardo, Carlota Costa, Beatriz Bellosillo, et al.
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