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Leukemia
|
September 1, 1996
A low rate of loss of heterozygosity is found at many different loci in childhood B-lineage acute lymphocytic leukemia
H Cavé, C Guidal, J Elion, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
September 1, 1995
Heterogeneity within the first constant segment of the major outer membrane protein gene in Chlamydia trachomatis serovar D/Da distinguishes 2 lineages
C Sayada, E Vretou, J Orfila, et al.
FEMS Microbiology Letters
|
September 15, 1991
Rapid genotyping of the Chlamydia trachomatis major outer membrane protein by the polymerase chain reaction
C Sayada, E Denamur, J Orfila, et al.
Human Mutation
|
January 1, 1997
Novel mutation (A141D) in exon 4 of the CFTR gene identified in an Algerian patient
L Gouya, O Pascaud, A Munck, et al.
Journal of Molecular Evolution
|
October 1, 1995
Sex in Escherichia coli does not disrupt the clonal structure of the population: evidence from random amplified polymorphic DNA and restriction-fragment-length polymorphism
P Desjardins, B Picard, B Kaltenböck, et al.
Journal of Clinical Microbiology
|
November 14, 1997
Virulence patterns of Escherichia coli K1 strains associated with neonatal meningitis
E Bingen, S Bonacorsi, N Brahimi, et al.
Journal of Medical Microbiology
|
May 1, 1994
Genetic heterogeneity of Pseudomonas aeruginosa clinical isolates revealed by esterase electrophoretic polymorphism and restriction fragment length polymorphism of the ribosomal RNA gene region
B Picard, E Denamur, A Barakat, et al.
Annales De Pediatrie
|
June 1, 1992
[HbD Iran-beta-thalassemia association in a Tunisian family]
F Guemira, S Abbes, R Ducrocq, et al.
Clinical Chemistry
|
February 1, 1985
Evidence for nonenzymic glycation of antithrombin III in diabetic patients
R Ducrocq, H Bachour, R Belkhodja, et al.
Journal of Medical Genetics
|
April 5, 2003
Prevalence of SMN1 deletion and duplication in carrier and normal populations: implication for genetic counselling
V Cusin, O Clermont, B Gérard, et al.
Page
of 19
Search research articles
Search
Showing results (41-50 of 189) with videos related to
Sort By:
Page
of 19
Leukemia
|
September 1, 1996
A low rate of loss of heterozygosity is found at many different loci in childhood B-lineage acute lymphocytic leukemia
H Cavé, C Guidal, J Elion, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
September 1, 1995
Heterogeneity within the first constant segment of the major outer membrane protein gene in Chlamydia trachomatis serovar D/Da distinguishes 2 lineages
C Sayada, E Vretou, J Orfila, et al.
FEMS Microbiology Letters
|
September 15, 1991
Rapid genotyping of the Chlamydia trachomatis major outer membrane protein by the polymerase chain reaction
C Sayada, E Denamur, J Orfila, et al.
Human Mutation
|
January 1, 1997
Novel mutation (A141D) in exon 4 of the CFTR gene identified in an Algerian patient
L Gouya, O Pascaud, A Munck, et al.
Journal of Molecular Evolution
|
October 1, 1995
Sex in Escherichia coli does not disrupt the clonal structure of the population: evidence from random amplified polymorphic DNA and restriction-fragment-length polymorphism
P Desjardins, B Picard, B Kaltenböck, et al.
Journal of Clinical Microbiology
|
November 14, 1997
Virulence patterns of Escherichia coli K1 strains associated with neonatal meningitis
E Bingen, S Bonacorsi, N Brahimi, et al.
Journal of Medical Microbiology
|
May 1, 1994
Genetic heterogeneity of Pseudomonas aeruginosa clinical isolates revealed by esterase electrophoretic polymorphism and restriction fragment length polymorphism of the ribosomal RNA gene region
B Picard, E Denamur, A Barakat, et al.
Annales De Pediatrie
|
June 1, 1992
[HbD Iran-beta-thalassemia association in a Tunisian family]
F Guemira, S Abbes, R Ducrocq, et al.
Clinical Chemistry
|
February 1, 1985
Evidence for nonenzymic glycation of antithrombin III in diabetic patients
R Ducrocq, H Bachour, R Belkhodja, et al.
Journal of Medical Genetics
|
April 5, 2003
Prevalence of SMN1 deletion and duplication in carrier and normal populations: implication for genetic counselling
V Cusin, O Clermont, B Gérard, et al.
Page
of 19