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American Journal of Human Genetics
|
June 13, 1998
Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database
C Jeanpierre, E Denamur, I Henry, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 9, 2001
[Neonatal screening of sickle cell anemia in metropolitan France]
J Bardakjian, M Benkerrou, F Bernaudin, et al.
American Journal of Hematology
|
January 12, 2000
Atypical beta(s) haplotypes are generated by diverse genetic mechanisms
M A Zago, W A Silva, B Dalle, et al.
Human Mutation
|
November 26, 1999
Compound SFTPB 1549C-->GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency
M Tredano, R M van Elburg, A G Kaspers, et al.
Annales De Genetique
|
January 1, 1997
Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded children
B Gérard, M F Le Heuzey, G Brunie, et al.
European Journal of Haematology
|
September 28, 2000
Acute clinical events in 299 homozygous sickle cell patients living in France. French Study Group on Sickle Cell Disease
M G Neonato, M Guilloud-Bataille, P Beauvais, et al.
Journal of Pediatric Hematology/Oncology
|
July 1, 1997
Three-year follow-up of hydroxyurea treatment in severely ill children with sickle cell disease. The French Study Group on Sickle Cell Disease
M de Montalembert, M Belloy, F Bernaudin, et al.
American Journal of Physical Anthropology
|
July 28, 1999
Genetic diversity of two African and sixteen South American populations determined on the basis of six hypervariable loci
W A Da Silva, M C Bortolini, D Meyer, et al.
European Journal of Haematology
|
April 25, 2000
Iron overload in thalassaemias and genetic haemochromatosis
P Aguilar-Martinez, J F Schved, C Badens, et al.
Page
of 19
Search research articles
Search
Showing results (181-190 of 189) with videos related to
Sort By:
Page
of 19
You have reached the last page of results.
This site can display upto 189 results.
American Journal of Human Genetics
|
June 13, 1998
Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database
C Jeanpierre, E Denamur, I Henry, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 9, 2001
[Neonatal screening of sickle cell anemia in metropolitan France]
J Bardakjian, M Benkerrou, F Bernaudin, et al.
American Journal of Hematology
|
January 12, 2000
Atypical beta(s) haplotypes are generated by diverse genetic mechanisms
M A Zago, W A Silva, B Dalle, et al.
Human Mutation
|
November 26, 1999
Compound SFTPB 1549C-->GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency
M Tredano, R M van Elburg, A G Kaspers, et al.
Annales De Genetique
|
January 1, 1997
Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded children
B Gérard, M F Le Heuzey, G Brunie, et al.
European Journal of Haematology
|
September 28, 2000
Acute clinical events in 299 homozygous sickle cell patients living in France. French Study Group on Sickle Cell Disease
M G Neonato, M Guilloud-Bataille, P Beauvais, et al.
Journal of Pediatric Hematology/Oncology
|
July 1, 1997
Three-year follow-up of hydroxyurea treatment in severely ill children with sickle cell disease. The French Study Group on Sickle Cell Disease
M de Montalembert, M Belloy, F Bernaudin, et al.
American Journal of Physical Anthropology
|
July 28, 1999
Genetic diversity of two African and sixteen South American populations determined on the basis of six hypervariable loci
W A Da Silva, M C Bortolini, D Meyer, et al.
European Journal of Haematology
|
April 25, 2000
Iron overload in thalassaemias and genetic haemochromatosis
P Aguilar-Martinez, J F Schved, C Badens, et al.
Page
of 19