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Progress in Clinical and Biological Research
|
January 1, 1989
Characterisation of a 3.5 kb deletion removing the alpha 1 globin gene
A E Kulozik
Klinische Padiatrie
|
July 1, 1991
[Beta thalassemia: molecular pathogenesis and clinical variability]
A E Kulozik
European Journal of Pediatrics
|
February 1, 1992
Beta-thalassaemia: molecular pathogenesis and clinical variability
A E Kulozik
Klinische Padiatrie
|
November 27, 2004
[Scientific results in paediatric oncology and haematology]
U Göbel, A E Kulozik
Klinische Padiatrie
|
May 12, 2006
[Genetic modifiers of homozygous sickle cell disease]
K Hartmann, A E Kulozik
Klinische Padiatrie
|
November 27, 2004
mRNA Metabolism and hereditary disorders: a tale of surveillance and escape
G Neu-Yilik, A E Kulozik
European Journal of Haematology
|
July 1, 1990
Relationship of foetal haemoglobin levels and beta s haplotypes in homozygous sickle cell disease
A G Falusi, A E Kulozik
Cell
|
February 20, 1999
A perfect message: RNA surveillance and nonsense-mediated decay
M W Hentze, A E Kulozik
Geburtshilfe Und Frauenheilkunde
|
April 1, 1993
[Monitoring pregnant patients from risk countries with sickle cell disease and thalassemia. Clinical aspects, screening and prenatal diagnosis]
R Dickerhoff, A E Kulozik, E Kohne
Acta Haematologica
|
August 21, 2002
Chronic haemolytic anaemia and glucose-6 phosphate dehydrogenase deficiency. Case report and review of the literature
P Hundsdoerfer, B Vetter, A E Kulozik
Page
of 6
Search research articles
Search
Showing results (1-10 of 60) with videos related to
Sort By:
Page
of 6
Progress in Clinical and Biological Research
|
January 1, 1989
Characterisation of a 3.5 kb deletion removing the alpha 1 globin gene
A E Kulozik
Klinische Padiatrie
|
July 1, 1991
[Beta thalassemia: molecular pathogenesis and clinical variability]
A E Kulozik
European Journal of Pediatrics
|
February 1, 1992
Beta-thalassaemia: molecular pathogenesis and clinical variability
A E Kulozik
Klinische Padiatrie
|
November 27, 2004
[Scientific results in paediatric oncology and haematology]
U Göbel, A E Kulozik
Klinische Padiatrie
|
May 12, 2006
[Genetic modifiers of homozygous sickle cell disease]
K Hartmann, A E Kulozik
Klinische Padiatrie
|
November 27, 2004
mRNA Metabolism and hereditary disorders: a tale of surveillance and escape
G Neu-Yilik, A E Kulozik
European Journal of Haematology
|
July 1, 1990
Relationship of foetal haemoglobin levels and beta s haplotypes in homozygous sickle cell disease
A G Falusi, A E Kulozik
Cell
|
February 20, 1999
A perfect message: RNA surveillance and nonsense-mediated decay
M W Hentze, A E Kulozik
Geburtshilfe Und Frauenheilkunde
|
April 1, 1993
[Monitoring pregnant patients from risk countries with sickle cell disease and thalassemia. Clinical aspects, screening and prenatal diagnosis]
R Dickerhoff, A E Kulozik, E Kohne
Acta Haematologica
|
August 21, 2002
Chronic haemolytic anaemia and glucose-6 phosphate dehydrogenase deficiency. Case report and review of the literature
P Hundsdoerfer, B Vetter, A E Kulozik
Page
of 6