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American Journal of Medical Genetics
|
July 31, 2001
Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2
F Martínez, I Martínez-Garay, J M Millán, et al.
Medicina Clinica
|
May 5, 1990
[Genetic analysis of Friedreich's ataxia using polymorphic DNA markers]
F Palau, J J Vílchez, M Beneyto, et al.
Archivos De La Sociedad Espanola De Oftalmologia
|
February 10, 2018
Which are the colors of the dress? Review of an atypical optic illusion
J González Martín-Moro, F Prieto Garrido, F Gómez Sanz, et al.
Anales Espanoles De Pediatria
|
March 1, 1997
[The evaluation of autopsy in the pediatric intensive unit]
A Castellanos Ortega, F Ortiz Melón, M García Fuentes, et al.
Revista Espanola De Cardiologia
|
January 1, 1973
[Holt-Oram syndrome. Report of a sporadic case]
M Peris Monfort, F J Algarra Vidal, F Prieto García, et al.
Clinical Genetics
|
February 28, 2004
Intronic L1 insertion and F268S, novel mutations in RPS6KA3 (RSK2) causing Coffin-Lowry syndrome
I Martínez-Garay, M J Ballesta, S Oltra, et al.
Medical and Pediatric Oncology
|
January 1, 1992
Acute nonlymphoblastic leukemia in children treated for acute lymphoblastic leukemia with an intensive regimen including teniposide
A Verdeguer, J G Ruiz, J Ferris, et al.
European Journal of Clinical Nutrition
|
September 1, 1993
Changes in diet and mortality from selected cancers in southern Mediterranean countries, 1960-1989
L Serra-Majem, C La Vecchia, L Ribas-Barba, et al.
Sangre
|
January 1, 1976
[Chromosome abnormalities in refractory anaemia with partial myeloblastosis (author's transl)]
F Prieto, L Badia, J R Calabuig, et al.
Medicina Intensiva
|
April 28, 2015
[Acute pericardial syndromes in the intensive care unit]
F Prieto-Valderrey, A Ferrezuelo-Mata, M N Parias-Angel, et al.
Page
of 16
Search research articles
Search
Showing results (121-130 of 157) with videos related to
Sort By:
Page
of 16
American Journal of Medical Genetics
|
July 31, 2001
Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2
F Martínez, I Martínez-Garay, J M Millán, et al.
Medicina Clinica
|
May 5, 1990
[Genetic analysis of Friedreich's ataxia using polymorphic DNA markers]
F Palau, J J Vílchez, M Beneyto, et al.
Archivos De La Sociedad Espanola De Oftalmologia
|
February 10, 2018
Which are the colors of the dress? Review of an atypical optic illusion
J González Martín-Moro, F Prieto Garrido, F Gómez Sanz, et al.
Anales Espanoles De Pediatria
|
March 1, 1997
[The evaluation of autopsy in the pediatric intensive unit]
A Castellanos Ortega, F Ortiz Melón, M García Fuentes, et al.
Revista Espanola De Cardiologia
|
January 1, 1973
[Holt-Oram syndrome. Report of a sporadic case]
M Peris Monfort, F J Algarra Vidal, F Prieto García, et al.
Clinical Genetics
|
February 28, 2004
Intronic L1 insertion and F268S, novel mutations in RPS6KA3 (RSK2) causing Coffin-Lowry syndrome
I Martínez-Garay, M J Ballesta, S Oltra, et al.
Medical and Pediatric Oncology
|
January 1, 1992
Acute nonlymphoblastic leukemia in children treated for acute lymphoblastic leukemia with an intensive regimen including teniposide
A Verdeguer, J G Ruiz, J Ferris, et al.
European Journal of Clinical Nutrition
|
September 1, 1993
Changes in diet and mortality from selected cancers in southern Mediterranean countries, 1960-1989
L Serra-Majem, C La Vecchia, L Ribas-Barba, et al.
Sangre
|
January 1, 1976
[Chromosome abnormalities in refractory anaemia with partial myeloblastosis (author's transl)]
F Prieto, L Badia, J R Calabuig, et al.
Medicina Intensiva
|
April 28, 2015
[Acute pericardial syndromes in the intensive care unit]
F Prieto-Valderrey, A Ferrezuelo-Mata, M N Parias-Angel, et al.
Page
of 16