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Annals of Hematology
|
March 23, 2001
Increased susceptibility of a carrier of X-linked chronic granulomatous disease (CGD) to Aspergillus fumigatus infection associated with age-related skewing of lyonization
A Rösen-Wolff, W Soldan, K Heyne, et al.
FEBS Letters
|
December 8, 2004
Identification of a putative p53 binding sequence within the human mitochondrial genome
K Heyne, S Mannebach, E Wuertz, et al.
European Journal of Pediatrics
|
March 1, 1997
Apolipoprotein J deficiency in types I and IV carbohydrate-deficient glycoprotein syndrome (glycanosis CDG)
K Heyne, H Henry, B Messerli, et al.
Hamostaseologie
|
June 4, 2014
[Computer aided dosage management of phenprocoumon anticoagulation therapy. Clinical validation]
R Dissmann, L J Cromme, A Salzwedel, et al.
Clinical Genetics
|
March 1, 1987
Roberts syndrome and SC phocomelia. A single genetic entity
C Römke, U Froster-Iskenius, K Heyne, et al.
The Journal of Laboratory and Clinical Medicine
|
April 1, 1997
Microheterogeneity of serum glycoproteins and their liver precursors in patients with carbohydrate-deficient glycoprotein syndrome type I: apparent deficiencies in clusterin and serum amyloid P
H Henry, J D Tissot, B Messerli, et al.
Journal of the National Cancer Institute
|
April 17, 1996
p53 expressions: predicting recurrence and second primary tumors in head and neck squamous cell carcinoma
D M Shin, J S Lee, S M Lippman, et al.
Nature Genetics
|
April 7, 1999
A human IFNGR1 small deletion hotspot associated with dominant susceptibility to mycobacterial infection
E Jouanguy, S Lamhamedi-Cherradi, D Lammas, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 58) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 58 results.
Annals of Hematology
|
March 23, 2001
Increased susceptibility of a carrier of X-linked chronic granulomatous disease (CGD) to Aspergillus fumigatus infection associated with age-related skewing of lyonization
A Rösen-Wolff, W Soldan, K Heyne, et al.
FEBS Letters
|
December 8, 2004
Identification of a putative p53 binding sequence within the human mitochondrial genome
K Heyne, S Mannebach, E Wuertz, et al.
European Journal of Pediatrics
|
March 1, 1997
Apolipoprotein J deficiency in types I and IV carbohydrate-deficient glycoprotein syndrome (glycanosis CDG)
K Heyne, H Henry, B Messerli, et al.
Hamostaseologie
|
June 4, 2014
[Computer aided dosage management of phenprocoumon anticoagulation therapy. Clinical validation]
R Dissmann, L J Cromme, A Salzwedel, et al.
Clinical Genetics
|
March 1, 1987
Roberts syndrome and SC phocomelia. A single genetic entity
C Römke, U Froster-Iskenius, K Heyne, et al.
The Journal of Laboratory and Clinical Medicine
|
April 1, 1997
Microheterogeneity of serum glycoproteins and their liver precursors in patients with carbohydrate-deficient glycoprotein syndrome type I: apparent deficiencies in clusterin and serum amyloid P
H Henry, J D Tissot, B Messerli, et al.
Journal of the National Cancer Institute
|
April 17, 1996
p53 expressions: predicting recurrence and second primary tumors in head and neck squamous cell carcinoma
D M Shin, J S Lee, S M Lippman, et al.
Nature Genetics
|
April 7, 1999
A human IFNGR1 small deletion hotspot associated with dominant susceptibility to mycobacterial infection
E Jouanguy, S Lamhamedi-Cherradi, D Lammas, et al.
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of 6