Manchester – Willink Biochemical Genetics Laboratory

Willink Biochemical Genetics Laboratory

Address
Willink Biochemical Genetics Laboratory
6th Floor, Pod 1, Manchester Centre for Genomic Medicine
St. Mary’s Hospital
Manchester University NHS Foundation Trust, Oxford Road
Manchester, M13 9WL

Website: https://www.mangen.co.uk/

Main Contact
Miss Teresa Hoi-Yee Wu
Consultant Clinical Scientist
T: (0161) 701 1838
F: (0161) 701 2303
E: Contact Miss Teresa Hoi-Yee Wu

Other Contacts

James Cooper

Oliver Parkes
Joint head of Newborn Screening and metabolites section
T: (0161)701 2140
F: (0161) 701 2303
E: Contact James Cooper and Oliver Parkes

Dr Heather Church
Principal Clinical Scientist ( Head of LSD section)
T: (0161)701 2306
F: (0161) 701 2303
E: Contact Dr Heather Church

Mrs Karen Tylee
Principal Clinical Scientist
T: (0161)701 2306
F: (0161) 701 2303
E: Contact Mrs Tykee Karen

Main BMS Contact
Mr Robert Gibson
Chief Biomedical Scientist
T: (0161)701 2143
F: (0161) 701 2303
E: Contact Mr Robert Gibson

LABORATORY INFORMATION


Clinical Pathology Accreditation (CPA): N/A

ISO15189: Full

UKAS No.: 9865

UKAS Website: Visit UKAS website


All | # A B C F G H I L M N O P S T V
There are currently 8 names in this directory beginning with the letter P.
Palmitoyl protein thioesterase 1 (Neuronal ceroid lipofuscinosis 1)
Whole blood [ EDTA ]

Phenylalanine/tyrosine (Phenylketonuria monitoring)
Plasma [ Lithium Heparin ] or Dried Bloodspot

Phytanate, phytanic acid (Peroxisomal disorders)
Plasma [ Lithium Heparin or EDTA ]

Plasma lysosomal enzymes (Mucolipidosis II (I-cell disease); mucolipidosis type III (pseudo-Hurler dystrophy))
Plasma [ EDTA ] or Fibroblasts

Plasmalogens (Peroxisomal disorders)
Whole blood [ EDTA ]

Pristanic acid, pristanate (peroxisomal disorders)
Plasma [ Lithium Heparin or EDTA ]

Propionyl Co A carboxylase
Fibroblasts

Pyruvate carboxylase (Pyruvate carboxylase deficiency)
Fibroblasts