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Results: 1-8 |
Results: 8
PREVALENCE OF THE FVQ506 (FACTOR-V-LEIDEN) MUTATION IN THE NORMAL ANDTHROMBOPHILIC ALGERIAN POPULATION
Authors: CHAFA O REGHIS A AUBERT A FISCHER AM
Citation: O. Chafa et al., PREVALENCE OF THE FVQ506 (FACTOR-V-LEIDEN) MUTATION IN THE NORMAL ANDTHROMBOPHILIC ALGERIAN POPULATION, British Journal of Haematology, 97(3), 1997, pp. 688-689
PRIMARY ADHALINOPATHY - A COMMON-CAUSE OF AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY OF VARIABLE SEVERITY
Authors: PICCOLO F ROBERDS SL JEANPIERRE M LETURCQ F AZIBI K BELDJORD C CARRIE A RECAN D CHAOUCH M REGHIS A ELKERCH F SEFIANI A VOIT T MERLINI L COLLIN H EYMARD B BECKMANN JS ROMERO NB TOME FMS FARDEAU M CAMPBELL KP KAPLAN JC
Citation: F. Piccolo et al., PRIMARY ADHALINOPATHY - A COMMON-CAUSE OF AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY OF VARIABLE SEVERITY, Nature genetics, 10(2), 1995, pp. 243-245
SCREENING FOR MUTATIONS IN FACTOR-VIII GENE USING THE SINGLE-STRAND CONFORMATION POLYMORPHISM
Authors: NAFA K MERIANE F CHELLALI T BENABADJI M REGHIS A VIEMONT M KAPLAN JC DELPECH M
Citation: K. Nafa et al., SCREENING FOR MUTATIONS IN FACTOR-VIII GENE USING THE SINGLE-STRAND CONFORMATION POLYMORPHISM, Human mutation, 5(4), 1995, pp. 357-359
SEVERE HYPOFIBRINOGENEMIA ASSOCIATED WITH BILATERAL ISCHEMIC NECROSISOF TOES AND FINGERS
Authors: CHAFA O CHELLALI T STERNBERG C REGHIS A HAMLADJI RM FISCHER AM
Citation: O. Chafa et al., SEVERE HYPOFIBRINOGENEMIA ASSOCIATED WITH BILATERAL ISCHEMIC NECROSISOF TOES AND FINGERS, Blood coagulation & fibrinolysis, 6(6), 1995, pp. 549-552
SEVERE HYPOFIBRINOGENEMIA ASSOCIATED WITH BILATERAL ISCHEMIC NECROSISOF TOES AND FINGERS
Authors: CHAFA O CHELLALI T STERNBERG C REGHIS A FISCHER AM
Citation: O. Chafa et al., SEVERE HYPOFIBRINOGENEMIA ASSOCIATED WITH BILATERAL ISCHEMIC NECROSISOF TOES AND FINGERS, Thrombosis and haemostasis, 73(6), 1995, pp. 1421-1421
A 13NT DELETION IN EXON-2 OF THE ALPHA-2 GLOBIN GENE - A NOVEL ALPHA-THALASSEMIA DEFECT IN ALGERIA
Authors: TAMOUZA R HARTEVELD K MERGHOUB T LAPOUMEROULIE C REGHIS A LABIE D BERNINI L ELION J
Citation: R. Tamouza et al., A 13NT DELETION IN EXON-2 OF THE ALPHA-2 GLOBIN GENE - A NOVEL ALPHA-THALASSEMIA DEFECT IN ALGERIA, Blood, 86(10), 1995, pp. 2609-2609
AT LEAST 5 POLYMORPHIC MUTANTS ACCOUNT FOR THE PREVALENCE OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY IN ALGERIA
Authors: NAFA K REGHIS A OSMANI N BAGHLI L AITABBES H BENABADJI M KAPLAN JC VULLIAMY T LUZZATTO L
Citation: K. Nafa et al., AT LEAST 5 POLYMORPHIC MUTANTS ACCOUNT FOR THE PREVALENCE OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY IN ALGERIA, Human genetics, 94(5), 1994, pp. 513-517
SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY WITH THE DEFICIENCY OF THE 50 KDA DYSTROPHIN-ASSOCIATED GLYCOPROTEIN MAPS TO CHROMOSOME-13Q12
Authors: AZIBI K BACHNER L BECKMANN JS MATSUMURA K HAMOUDA E CHAOUCH M CHAOUCH A AITOUARAB R VIGNAL A WEISSENBACH J VINET MC LETURCQ F COLLIN H TOME FMS REGHIS A FARDEAU M CAMPBELL KP KAPLAN JC
Citation: K. Azibi et al., SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY WITH THE DEFICIENCY OF THE 50 KDA DYSTROPHIN-ASSOCIATED GLYCOPROTEIN MAPS TO CHROMOSOME-13Q12, Human molecular genetics, 2(9), 1993, pp. 1423-1428
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