Newborn Screening and Biochemical Genetics

In Newborn Screening and Biochemical Genetics, we provide biochemical testing and result interpretation for the diagnosis, monitoring and clinical care of patients with rare but serious conditions, including inherited metabolic disorders (inborn errors of metabolism).

Newborn Screening (NBS)

Inherited Metabolic Disorders (IMD)

Molecular Genetics


IMD laboratory 0121 333 9942

IMD Duty Biochemist – mobile phone via switchboard – 0121 333 9999

Screening Laboratory 0121 333 9905

Molecular Genetics 0121 333 9877


Department staff

The team

Meet the team

Find out about who works in this section...

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