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Haemophilia A
Duchenne Muscular Dystrophy in a Female Patient with a Karyotype of 46,X,I(X)(Q10)
5.1.1 OCR Exambuilder
Haemophilia A
Gene Therapy: the Promise of a Permanent Cure
Guidelines for the Management of Haemophilia in Australia
Regulation and Properties of Glucose-6-Phosphate Dehydrogenase: a Review
Spontaneous Deep Vein Thrombosis in Hemophilia A: a Case Report Murat Bicer, Murat Yanar* and Oktay Tuydes
Severe Haemophilia a in a Preterm Girl With
Hypoxanthine-Guanine Phosphoribosyltransferase. Genetic Evidence for Identical Mutations in Two Partially Deficient Subjects
Determinants and Modifiers of Bleeding Phenotypes in Haemophilia-A
The Clinical Landscape for AAV Gene Therapies
Pre-Implantation Genetic Diagnosis and Assisted Reproductive Technology in Haemophilia
Complications in Clotting Find out How Haemophilia Can
The Provision of Genetic Counselling Services for Haemophilia and Related Inherited Bleeding Conditions
The Bleeding Neonate
Mouse Models of Human Disease. Part II: Recent Progress and Future Directions
Youth Perspectives on Genetic Inheritance, Carrier Status and Disclosure
(G6PD) Deficiency Scientist D M.P.S.S.Singh Assistant Editors Dr
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
Carriers of Haemophilia
Roche Enters Into Definitive Merger Agreement to Acquire Spark Therapeutics
Atypical Bleeding Due to Idiopathic Thrombocytopenia in Association with Low Factor VIII Levels M F Riordan,Fghhill
Practice Guidelines for the Molecular Diagnosis of Haemophilia B
X Chromosome Inactivation in Carriers of Fabry Disease: Review and Meta-Analysis
Genetic Mapping of DNA Segments Relative to the Locus for the Fragile-X Syndrome at Xq27.3 L
Latest Chapter That Has Been Updated Is Related to Inhibitor Development
Gene Therapy Delivery to the Eye Leber’S Congenital Amaurosis – Gene Therapy
Immune Thrombocytopenia in a Case of Severe Congenital Hemophilia A: a Rare Clinical Scenario
Haemophilia A
Molecular Diagnosis of Haemophilia and Other Bleeding Disorders
Molecular Genetics of Hemophilia A: Clinical Perspectives
Genetics, Reproduction and Family Planning Many Genes Identified in Bleeding Disorders
Identification of the Profile of the Patients with Hemophilia B Eligible for Treatment with Nonacog Alfa Once-Weekly
Haemophilia a & Haemophilia B
Acquired Hemophilia in an Elderly Person
Identification and Basic Management of Bleeding Disorders in Adults
Improved Mutation Detection for Haemophilia a in South Africa 1
Mild Haemophilia A
Disease Gene Mapping in Isolated Human Populations: the Example of Finland
Haemophilia A
What Causes Genetic Conditions?
Sex Ratio of the Mutation Frequencies in Haemophilia A: Coagulation Assays and RFLP Analysis
Congenital Platelet Disorders Mike Makris Sheffield, UK Inherited Platelet Disorders
AAV-Based Gene Therapy Products: Ongoing Clinical Trials
Sex Ratio of the Mutation Frequencies in Haemophilia A: Estimation and Meta-Analysis