一个反复的蜂蜜蜂.

Same author

De novo mutation causing sporadic type 2A von Willebrancd's disease: report of three cases.

Haemophilia : the official journal of the World Federation of Hemophilia·2016

Same author

Cytolytic activity against mycobacterial antigens: differences between haemophiliacs with and without HIV infection.

Haemophilia : the official journal of the World Federation of Hemophilia·2016

Same author

The usefulness of bone marrow aspiration in the diagnosis of Niemann-Pick disease type C in infantile liver disease.

Archives of disease in childhood·2006

Same author

Down's syndrome and acute lymphoblastic leukaemia: clinical features and response to treatment.

Archives of disease in childhood·2001

Same author

Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of 3 different families with type 2A (phenotype IID) von Willebrand disease.

Blood·2001

Same author

Site and type of mutations in the factor VIII gene in patients and carriers of haemophilia A.

Haemophilia : the official journal of the World Federation of Hemophilia·2001

相关实验视频

一个反复的蜂蜜蜂.

相关概念视频

De novo mutation causing sporadic type 2A von Willebrancd's disease: report of three cases.

Cytolytic activity against mycobacterial antigens: differences between haemophiliacs with and without HIV infection.

The usefulness of bone marrow aspiration in the diagnosis of Niemann-Pick disease type C in infantile liver disease.

Down's syndrome and acute lymphoblastic leukaemia: clinical features and response to treatment.

Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of 3 different families with type 2A (phenotype IID) von Willebrand disease.

Site and type of mutations in the factor VIII gene in patients and carriers of haemophilia A.

相关实验视频

一个反复的蜂蜜蜂.

相关概念视频

De novo mutation causing sporadic type 2A von Willebrancd's disease: report of three cases.

Cytolytic activity against mycobacterial antigens: differences between haemophiliacs with and without HIV infection.

The usefulness of bone marrow aspiration in the diagnosis of Niemann-Pick disease type C in infantile liver disease.

Down's syndrome and acute lymphoblastic leukaemia: clinical features and response to treatment.

Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of 3 different families with type 2A (phenotype IID) von Willebrand disease.

Site and type of mutations in the factor VIII gene in patients and carriers of haemophilia A.

相关实验视频

一个反复的蜂蜜蜂.

相关概念视频

相关文章

De novo mutation causing sporadic type 2A von Willebrancd's disease: report of three cases.

Cytolytic activity against mycobacterial antigens: differences between haemophiliacs with and without HIV infection.

The usefulness of bone marrow aspiration in the diagnosis of Niemann-Pick disease type C in infantile liver disease.

Down's syndrome and acute lymphoblastic leukaemia: clinical features and response to treatment.

Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of 3 different families with type 2A (phenotype IID) von Willebrand disease.

Site and type of mutations in the factor VIII gene in patients and carriers of haemophilia A.

相关实验视频

一个反复的蜂蜜蜂.

相关概念视频

相关文章

De novo mutation causing sporadic type 2A von Willebrancd's disease: report of three cases.

Cytolytic activity against mycobacterial antigens: differences between haemophiliacs with and without HIV infection.

The usefulness of bone marrow aspiration in the diagnosis of Niemann-Pick disease type C in infantile liver disease.

Down's syndrome and acute lymphoblastic leukaemia: clinical features and response to treatment.

Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of 3 different families with type 2A (phenotype IID) von Willebrand disease.

Site and type of mutations in the factor VIII gene in patients and carriers of haemophilia A.