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Annales De Genetique
|
January 1, 1982
Sorbitol dehydrogenase (EC.1.1.1.14) polymorphism in human seminal plasma
B Ibarra, G Gonzalez-Quiroga, G Vaca, et al.
American Journal of Medical Genetics
|
January 1, 1980
Autosomal recessive spondylo-epi-metaphyseal dysplasia (Irapa type) in a Mexican family: delineation of the syndrome
A Hernández, M L Ramírez, Z Nazará, et al.
Optics Express
|
June 11, 2008
Initial development of supercontinuum in fibers with anomalous dispersion pumped by nanosecond-long pulses
N Korneev, E A Kuzin, B Ibarra-Escamilla, et al.
Revista De Neurologia
|
February 12, 1998
[Jugular megabulb as a cause of pulsatile tinnitus]
S Abilleira, F Romero-Vidal, J Alvarez-Sabín, et al.
Archivos De Investigacion Medica
|
January 1, 1980
Detection of hemoglobin alterations in a sample population in northwest Mexico. Preliminary report
B Ibarra, P Zúñiga, M L Ramírez, et al.
Annales De Genetique
|
January 1, 1980
A simple assay for uridine diphosphate galactose 4-epimerase activity
G Vaca, J Sanchez-Corona, N Olivares, et al.
Acta Cientifica Venezolana
|
January 1, 1988
Determination of iron, copper and zinc in human whole vitreous humor by flow injection atomic absorption spectrometry
J L Burguera, M Burguera, C Rivas, et al.
Clinical Genetics
|
June 1, 1987
Centric fission, centromere-telomere fusion and isochromosome formation: a possible origin of a de novo 12p trisomy
H Rivera, L García-Esquivel, M Jiménez-Sáinz, et al.
American Journal of Hematology
|
March 1, 1996
Haplotype analysis of the Mexican frameshift Cd 11 (-T) and -28 A->C beta-thalassemia alleles
F J Perea, M A Esparza, A R Villalobos-Arambula, et al.
Annales De Genetique
|
January 1, 1989
Screening for thermostability and electrophoretic red blood cell sorbitol dehydrogenase (E.C.1.1.1.14) variants
B Ibarra, G Vaca, F J Perea, et al.
Page
of 15
Search research articles
Search
Showing results (51-60 of 144) with videos related to
Sort By:
Page
of 15
Annales De Genetique
|
January 1, 1982
Sorbitol dehydrogenase (EC.1.1.1.14) polymorphism in human seminal plasma
B Ibarra, G Gonzalez-Quiroga, G Vaca, et al.
American Journal of Medical Genetics
|
January 1, 1980
Autosomal recessive spondylo-epi-metaphyseal dysplasia (Irapa type) in a Mexican family: delineation of the syndrome
A Hernández, M L Ramírez, Z Nazará, et al.
Optics Express
|
June 11, 2008
Initial development of supercontinuum in fibers with anomalous dispersion pumped by nanosecond-long pulses
N Korneev, E A Kuzin, B Ibarra-Escamilla, et al.
Revista De Neurologia
|
February 12, 1998
[Jugular megabulb as a cause of pulsatile tinnitus]
S Abilleira, F Romero-Vidal, J Alvarez-Sabín, et al.
Archivos De Investigacion Medica
|
January 1, 1980
Detection of hemoglobin alterations in a sample population in northwest Mexico. Preliminary report
B Ibarra, P Zúñiga, M L Ramírez, et al.
Annales De Genetique
|
January 1, 1980
A simple assay for uridine diphosphate galactose 4-epimerase activity
G Vaca, J Sanchez-Corona, N Olivares, et al.
Acta Cientifica Venezolana
|
January 1, 1988
Determination of iron, copper and zinc in human whole vitreous humor by flow injection atomic absorption spectrometry
J L Burguera, M Burguera, C Rivas, et al.
Clinical Genetics
|
June 1, 1987
Centric fission, centromere-telomere fusion and isochromosome formation: a possible origin of a de novo 12p trisomy
H Rivera, L García-Esquivel, M Jiménez-Sáinz, et al.
American Journal of Hematology
|
March 1, 1996
Haplotype analysis of the Mexican frameshift Cd 11 (-T) and -28 A->C beta-thalassemia alleles
F J Perea, M A Esparza, A R Villalobos-Arambula, et al.
Annales De Genetique
|
January 1, 1989
Screening for thermostability and electrophoretic red blood cell sorbitol dehydrogenase (E.C.1.1.1.14) variants
B Ibarra, G Vaca, F J Perea, et al.
Page
of 15