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Cancer Genetics and Cytogenetics|April 1, 1991
Chromosome 5 abnormalities in acute lymphoblastic leukemiaF Palau, F Prieto, L Badia, et al.Neuroepidemiology|January 1, 1995
Friedreich's ataxia: an epidemiological study in Valencia, Spain, based on consanguinity analysisJ M López-Arlandis, J J Vílchez, F Palau, et al.Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|October 25, 2017
Motion estimation of subcellular structures from fluorescence microscopy imagesA Vallmitjana, A Civera-Tregon, J Hoenicka, et al.Medicina Clinica|May 6, 1995
[The diagnosis and prevalence of locus CMT1A duplication in Charcot-Marie-Tooth disease type 1]S Bort, T Sevilla, J J Vílchez, et al.Prenatal Diagnosis|June 1, 1995
Prenatal diagnosis of Friedreich ataxia: improved accuracy by using new genetic flanking markersE Monros, P Smeyers, M A Ramos, et al.Neurologia (Barcelona, Spain)|May 3, 2001
[Neuroimaging study with morphometric analysis of hereditary and idiopathic ataxia]V Villanueva-Haba, M Garcés-Sánchez, L Bataller, et al.Cancer Genetics and Cytogenetics|January 1, 1991
Cytogenetic evidence of involvement of an early progenitor myeloid cell in 4;11 translocation-associated acute leukemiaF Palau, F Prieto, L Badia, et al.Journal of Medical Genetics|May 23, 1998
Genetic localisation of mental retardation with spastic diplegia to the pericentromeric region of the X chromosome: X inactivation in female carriersF Martínez, M Tomás, J M Millán, et al.Human Genetics|June 1, 1996
A family segregating a Friedreich ataxia phenotype that is not linked to the FRDA locusP Smeyers, E Monrós, J Vílchez, et al.Neurologia (Barcelona, Spain)|June 10, 2000
[Recurrent familial brachial plexopathy as the only clinical expression of neuropathy with susceptibility to pressure]E Gil-Néciga, E Franco, A Sánchez, et al.Pageof 6