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V Raynal

Showing results (11-20 of 16) with videos related to

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Blood|August 15, 1992
Multiple Rh messenger RNA isoforms are produced by alternative splicingC Le Van Kim, B Chérif-Zahar, V Raynal, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 15, 1992
Molecular cloning and primary structure of the human blood group RhD polypeptideC Le van Kim, I Mouro, B Chérif-Zahar, et al.
Blood|July 15, 1993
Structure and expression of the RH locus in the Rh-deficiency syndromeB Chérif-Zahar, V Raynal, C Le Van Kim, et al.
Nature Genetics|February 1, 1996
Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiencyB Cherif-Zahar, V Raynal, P Gane, et al.
British Journal of Haematology|September 30, 1998
Shift from Rh-positive to Rh-negative phenotype caused by a somatic mutation within the RHD gene in a patient with chronic myelocytic leukaemiaB Chérif-Zahar, V Bony, R Steffensen, et al.
Oncogene|January 19, 2011
The constitutive activity of the ALK mutated at positions F1174 or R1275 impairs receptor traffickingP Mazot, A Cazes, M C Boutterin, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Blood|August 15, 1992
Multiple Rh messenger RNA isoforms are produced by alternative splicingC Le Van Kim, B Chérif-Zahar, V Raynal, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 15, 1992
Molecular cloning and primary structure of the human blood group RhD polypeptideC Le van Kim, I Mouro, B Chérif-Zahar, et al.
Blood|July 15, 1993
Structure and expression of the RH locus in the Rh-deficiency syndromeB Chérif-Zahar, V Raynal, C Le Van Kim, et al.
Nature Genetics|February 1, 1996
Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiencyB Cherif-Zahar, V Raynal, P Gane, et al.
British Journal of Haematology|September 30, 1998
Shift from Rh-positive to Rh-negative phenotype caused by a somatic mutation within the RHD gene in a patient with chronic myelocytic leukaemiaB Chérif-Zahar, V Bony, R Steffensen, et al.
Oncogene|January 19, 2011
The constitutive activity of the ALK mutated at positions F1174 or R1275 impairs receptor traffickingP Mazot, A Cazes, M C Boutterin, et al.
Pageof 2