Molecular Haemostasis & Thrombosis

Molecular Haemostasis & Thrombosis
Synnovis Analytics LLP - Guy's and St. Thomas' NHS Foundation Trust
St. Thomas' Hospital, Westminster Bridge Road
London, Greater London, United Kingdom SE1 7EH
Phone: +44 207 188 2798
Fax: +44 207 188 9797
Email: mike.mitchell@gstt.nhs.uk
Online Contact: https://southeastgenomics.nhs.uk/glh/haem/
Website: https://www.synnovis.co.uk/departments-and-laboratories/molecular-haemostasis-laboratory-at-st-thomas

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GTR Lab ID: 304136, Last updated:2024-10-31

Personnel

Director: Mike Mitchell, PhD, MS, Lab Director
Phone: +44 207 188 6817
Fax: +44 207 401 3125
Email: mike.mitchell@gstt.nhs.uk

Conditions and tests

32 conditions/phenotypes with 20 tests
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AA amyloidosis1 test
Afibrinogenemia1 test
Bernard Soulier syndrome1 test
Bernard-Soulier syndrome, type A1 test
Classic homocystinuria1 test
Combined deficiency of factor V and factor VIII1 test
Congenital prothrombin deficiency1 test
Factor 5 and Factor VIII, combined deficiency of, 21 test
Factor V deficiency1 test
Factor VII deficiency2 tests
Factor X deficiency1 test
Factor XIII, A subunit, deficiency of1 test
Factor XIII, b subunit, deficiency of1 test
Glanzmann thrombasthenia1 test
Hereditary antithrombin deficiency1 test
Hereditary factor I deficiency disease1 test
Hereditary factor IX deficiency disease1 test
Hereditary factor VIII deficiency disease1 test
Hereditary factor XI deficiency disease1 test
Homocystinuria due to methylene tetrahydrofolate reductase deficiency1 test
Homocystinuria, pyridoxine-nonresponsive1 test
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss1 test
Thrombophilia due to protein C deficiency, autosomal dominant1 test
Thrombophilia due to protein C deficiency, autosomal recessive1 test
Thrombophilia due to protein S deficiency, autosomal dominant1 test
Thrombophilia due to protein S deficiency, autosomal recessive1 test
von Willebrand disease type 11 test
Von Willebrand disease type 2A1 test
Von Willebrand disease type 2B1 test
von Willebrand disease type 2M1 test
von Willebrand disease type 2N1 test
von Willebrand disease type 31 test

List of services

Clinical Testing/Confirmation of Mutations Identified Previously
Confirmation of research findings
Custom Deletion/Duplication Testing
Prenatal testing
Custom Sequence Analysis
Carrier testing
Mutation Confirmation

List of certifications/licenses

Certifications

CPA, Number: 8595, Expiration date: 2024-11-27

Participation in external programs

Standardization programs

Locus-specific Databases
Mutation-specific Databases

Data exchange Programs

Locus-specific Databases
Mutation-specific Databases

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