Haemophilia A
Top View
- Acquired Bleeding Disorders
- FRACP Lecture Series AGENDA Investigations Haemophilia
- MOLECULAR BASIS of GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY in CAPE COAST, GHANA by Dan Osei Mensah Bonsu, B.Sc. Human Biolo
- Policy Brief 006B.Pdf
- Gene Therapy
- Identification of a Two Base Pair Deletion in Five Unrelated Families with Adrenoleukodystrophy
- Bleeding Thrombotic and Platelet Disorder TIER1 Genes (V.ISTH 2019.1)
- The Bleeding Child; Is It NAI? a E Thomas
- Bleeding Disorders in Orthopedic Surgery
- Symptomatic Carriers of Hemophilia
- Heritable Skewed X-Chromosome Inactivation Leads to Haemophilia a Expression in Heterozygous Females
- Genetic Counselling in Haemophilia by Discriminant Analysis 1975-1980*
- Familial Skewed X Chromosome Inactivation in Adrenoleukodystrophy Manifesting Heterozygotes from a Chinese Pedigree
- Understanding Haemophilia
- Moderate Haemophilia B
- In Hemophilia a with Or Without Factor Viii Inhibitors
- Haemophilia A: from Mutation Analysis to New Therapies
- How to Discuss Gene Therapy for Haemophilia? a Patient and Physician Perspective