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Results of search for 'au:"Robledo, M"', page 3 of 7
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Authors
Albertos, J
Arranz, E
Ayuso, C
Barroso, A
Benitez, J
Benítez, J
Calle, G
Cascón, A
Cebrián, A
Echezarreta, G
Gutiérrez, F
Martínez, B
Martínez-Delgado, B
Osorio, A
Restrepo, A
Rivas, C
Robledo, M
Robledo, M A
Robledo, M M
Rodríguez-Antona, C
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41.
Paracoccidioidomycosis, (South American blastomycosis). A study of 39 cases observed in Medellin, Colombia.
[electronic resource]
by
Restrepo, A
Robledo, M
Gutiérrez, F
Sanclemente, M
Castañeda, E
Calle, G
Producer:
19700414
In:
The American journal of tropical medicine and hygiene
vol. 19
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42.
Sebaceous glands and hair follicles in the cervix uteri.
[electronic resource]
by
Robledo, M C
Vazquez, J J
Contreras-Mejuto, F
Lopez-Garcia, G
Producer:
19921103
In:
Histopathology
vol. 21
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43.
[Detection of monoclonality in non-Hodgkin's B-cell lymphomas using PCR].
[electronic resource]
by
Robledo, M
Martínez, B
Arranz, E
Marcos, B
Rivas, C
Benítez, J
Producer:
19941110
In:
Sangre
vol. 39
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44.
SDHB mutation analysis in familial and sporadic phaeochromocytoma identifies a novel mutation.
[electronic resource]
by
Cascón, A
Cebrián, A
Ruiz-Llorente, S
Tellería, D
Benítez, J
Robledo, M
Producer:
20021213
In:
Journal of medical genetics
vol. 39
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45.
Rearrangement of one RAR-alpha gene in an acute promyelocytic leukemia case with t(15;17) and t(6;17) involving chromosomes 17 band q21.
[electronic resource]
by
Arranz, E
López, J L
Robledo, M
Martínez, B
Escudero, A
Benítez, J
Producer:
19960621
In:
Cancer genetics and cytogenetics
vol. 87
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46.
[Asymptomatic patient and lung alteration].
[electronic resource]
by
Godoy Mayoral, R
López Miguel, P
Fernández Robledo, M E
Nuñez Ares, A
Producer:
20090915
In:
Revista clinica espanola
vol. 209
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47.
Subcutaneous phycomycosis: report of the first case observed in Colombia, South America.
[electronic resource]
by
Restrepo, A
Greer, D L
Robledo, M
Diaz, C
Lopez, R
Bravo, C
Producer:
19670602
In:
The American journal of tropical medicine and hygiene
vol. 16
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48.
Detection of trisomy 8 using conventional cytogenetic techniques and interphase FISH analysis in 34 myeloid disorders: a comparative study.
[electronic resource]
by
Arranz, E
Robledo, M
Martínez, B
Prieto, E
Portero, J A
Benítez, J
Producer:
19970501
In:
Cancer genetics and cytogenetics
vol. 94
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49.
[Oxyphillic adenoma as a cause of primary hyperparathyroidism].
[electronic resource]
by
Barrios, J A
Robledo, M C
Contreras, F
Alvarez-Cienfuegos, J
Voltas, J
Producer:
19910909
In:
Revista de medicina de la Universidad de Navarra
vol. 34
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50.
Trinucleotide (CAG) repeat expansion in chromosomes of Spanish patients with Huntington's disease.
[electronic resource]
by
Benitez, J
Fernandez, E
Garcia Ruiz, P
Robledo, M
Ramos, C
Yébenes, J
Producer:
19941215
In:
Human genetics
vol. 94
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51.
[Cephalometry in rehabilitation].
[electronic resource]
by
Cortés, N
Robledo, M F
Cuartas, M E
Giraldo, O L
Vélez, M T
Producer:
19911114
In:
Revista de la Facultad de Odontologia Universidad de Antioquia
vol. 2
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52.
Incidence of homogeneously staining regions in non-Hodgkin lymphomas.
[electronic resource]
by
Arranz, E
Robledo, M
Martínez, B
Gallego, J
Román, A
Rivas, C
Benítez, J
Producer:
19960725
In:
Cancer genetics and cytogenetics
vol. 87
Online resources:
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53.
[Spinocerebellar ataxia type VII (AEC 7). Report of a Spanish family with the disease].
[electronic resource]
by
Mayo, D
Yusta, A
Vázquez, J M
García-Ruiz, P
Robledo, M
Benítez, J
Producer:
19991229
In:
Revista de neurologia
vol. 28
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54.
[Identification of a de novo mutation in a patient without von Hippel-Lindau syndrome: clinical and diagnostic implications].
[electronic resource]
by
Cebrián, A
Ruiz Barnés, P
Osorio, A
Martínez-Delgado, B
Benítez, J
Robledo, M
Producer:
19991213
In:
Neurologia (Barcelona, Spain)
vol. 14
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55.
Molecular analysis of the six most recurrent mutations in the BRCA1 gene in 87 Spanish breast/ovarian cancer families.
[electronic resource]
by
Osorio, A
Robledo, M
Albertos, J
Díez, O
Alonso, C
Baiget, M
Benítez, J
Producer:
19980319
In:
Cancer letters
vol. 123
Online resources:
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56.
[A clinical, cytogenetic and molecular study of 10 patients with the Prader-Willi syndrome].
[electronic resource]
by
Barabash, A
Robledo, M
Sanz, R
Renedo, M
Ramos, C
Ayuso, C
Benítez, J
Producer:
19970423
In:
Medicina clinica
vol. 108
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57.
Immunophenotypic and Gene Rearrangement Analysis in Null- or T-Cell Neoplasias: Study of 16 Cases.
[electronic resource]
by
Santos, M
Rivas, C
Echezarreta, G
Bernacer, M
Santon, A
Robledo, M
Benitez, J
Producer:
20160730
In:
Leukemia & lymphoma
vol. 4
Online resources:
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58.
[The gene responsible for Huntington's disease in Spanish families: its diagnostic value and the relation between trinucleotide expansion and the clinical characteristics].
[electronic resource]
by
Benítez, J
Fernández, E
García Ruiz, P
Robledo, M
Ayuso, C
García Yébenes, J
Producer:
19941116
In:
Revista clinica espanola
vol. 194
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59.
Polymorphic variations in peripherin-RDS gene in the Spanish population.
[electronic resource]
by
Trujillo, M J
Ayuso, C
Robledo, M
Sandoval, B G
Ramos, C
Benitez, J
Producer:
19960625
In:
Annales de genetique
vol. 38
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60.
Application of cellular ELISA (CELISA) to the detection of human monoclonal autoantibodies.
[electronic resource]
by
Sánchez, B
Melero, J
Robledo, M M
Tarragó, D
Yélamos, J
González, M F
Producer:
19940114
In:
Human antibodies and hybridomas
vol. 4
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