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Hereditary Diseases And Blood Transfusion, Vol. 30 Book

Hereditary Diseases And Blood Transfusion, Vol. 30
Hereditary Diseases And Blood Transfusion, Vol. 30, The discovery of the structure and function of DNA and the cracking of the genetic code have led to rapid advances in gene therapy and screening and diagnosis on a molecular basis. While initial therapy has been for patients with single gene defects, ther, Hereditary Diseases And Blood Transfusion, Vol. 30 has a rating of 3 stars
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Hereditary Diseases And Blood Transfusion, Vol. 30, The discovery of the structure and function of DNA and the cracking of the genetic code have led to rapid advances in gene therapy and screening and diagnosis on a molecular basis. While initial therapy has been for patients with single gene defects, ther, Hereditary Diseases And Blood Transfusion, Vol. 30
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  • Hereditary Diseases And Blood Transfusion, Vol. 30
  • Written by author C. Th Smit Sibinga
  • Published by Springer-Verlag New York, LLC, September 1995
  • The discovery of the structure and function of DNA and the cracking of the genetic code have led to rapid advances in gene therapy and screening and diagnosis on a molecular basis. While initial therapy has been for patients with single gene defects, ther
  • The discovery of the structure and function of DNA and the cracking of the genetic code have led to rapid advances in gene therapy and screening and diagnosis on a molecular basis. While initial therapy has been for patients with single gene defects, ther
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Foreword
The Molecular Biology of Haemophilia3
Molecular Biology of the Various Types of Von Willebrand Disease11
Molecular Basis of Thrombophilia25
Inhibitory Sequences Within the Clotting Factor VIII cDNA Block Transcriptional Elongation and Complicate Efforts Toward Gene Therapy for Haemophilia A31
Globin Gene Regulation53
Molecular Pathology of the Thalassaemia Syndromes63
The Current Status of Bone Marrow Transplantation and Gene Therapy in the Management of TheHaemoglobinopathies71
The Molecular Biology of Blood Groups: Relevance to the Study of Erythroid Maturation and the Clinical Management of Haemolytic Disease of the Newborn81
Genetic Abnormalities in Blood Group Serology93
The Role of The Blood Bank in Human Gene Therapy Trials117
Translocation in Cancer: Mechanism of Oncogenic Conversion and Implications for Therapy131
Role of Topoisomerase II A and B Isozymes in Determining Drug Resistance In Vitro and In Vivo145
Impact of Cell Culture Technology on Transfusion Medicine153
Gene Therapy for Primary Immune Deficiencies167
Ethics and Genetic Manipulation183
Is There a Role for Transfusion Medicine in the Genetic Correction of Genetic Disorders and Other Diseases?189
Vectors for Gene Therapy: Strategies for Making Gene Therapy Work209
From Blood Stain to Pathogenesis Study of Human Hereditary Diseases223
The Potential Impact of Gene Therapy in Blood Transfusion233
Index251


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Hereditary Diseases And Blood Transfusion, Vol. 30, The discovery of the structure and function of DNA and the cracking of the genetic code have led to rapid advances in gene therapy and screening and diagnosis on a molecular basis. While initial therapy has been for patients with single gene defects, ther, Hereditary Diseases And Blood Transfusion, Vol. 30

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Hereditary Diseases And Blood Transfusion, Vol. 30, The discovery of the structure and function of DNA and the cracking of the genetic code have led to rapid advances in gene therapy and screening and diagnosis on a molecular basis. While initial therapy has been for patients with single gene defects, ther, Hereditary Diseases And Blood Transfusion, Vol. 30

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Hereditary Diseases And Blood Transfusion, Vol. 30, The discovery of the structure and function of DNA and the cracking of the genetic code have led to rapid advances in gene therapy and screening and diagnosis on a molecular basis. While initial therapy has been for patients with single gene defects, ther, Hereditary Diseases And Blood Transfusion, Vol. 30

Hereditary Diseases And Blood Transfusion, Vol. 30

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