| Phrase | Consultant | Town | Special Interests |
| Cancer genetics | *Consultant(s)* | *Towns* | Cancer genetics, paediatric genetics, neurofibromatosis type 1 |
Cancer genetics | *Consultant(s)* | *Towns* | Cancer genetics, paediatric genetics, Huntington's disease | cancer genetics | *Consultant(s)* | *Towns* | Prenatal diagnosis, genetic eye problems, cancer genetics | cardiac genetics | *Consultant(s)* | *Towns* | Paediatric genetics, cardiac genetics, rare disease genetics | Cardiac genetics | *Consultant(s)* | *Towns* | Cardiac genetics | Clinical Genetics | *Consultant(s)* | *Towns* | Disorders of genomic imprinting in humans, genetics of recessive diseases in consanguineous families, molecular genetics of ketohexokinase | Clinical Genetics | *Consultant(s)* | *Towns* | Skeletal dysplasia, paediatric genetics | Clinical Genetics | *Consultant(s)* | *Towns* | Paediatric genetics, renal genetics, prenatal genetics | Clinical Genetics | *Consultant(s)* | *Towns* | Paediatric genetics, cardiac genetics, rare disease genetics | Clinical Genetics | *Consultant(s)* | *Towns* | Dysmorphology, Huntington's disease | Clinical Genetics | *Consultant(s)* | *Towns* | Cancer genetics, paediatric genetics, neurofibromatosis type 1 | Clinical Genetics | *Consultant(s)* | *Towns* | Cancer genetics, paediatric genetics, Huntington's disease | Clinical Genetics | *Consultant(s)* | *Towns* | Cardiac genetics | Clinical Genetics | *Consultant(s)* | *Towns* | Prenatal diagnosis, genetic eye problems, cancer genetics | genetics and psychopharmacology of psychoses and bipolar disorder | *Consultant(s)* | *Towns* | Bipolar affective disorders, psychosis, genetics and psychopharmacology of psychoses and bipolar disorder | genetics of premature myocardial infarction | *Consultant(s)* | *Towns* | Academic cardiology, genetics of premature myocardial infarction, myocardial infarction, congenital heart disease, epidemiology | genetics of recessive diseases in consanguineous families | *Consultant(s)* | *Towns* | Disorders of genomic imprinting in humans, genetics of recessive diseases in consanguineous families, molecular genetics of ketohexokinase | molecular genetics of ketohexokinase | *Consultant(s)* | *Towns* | Disorders of genomic imprinting in humans, genetics of recessive diseases in consanguineous families, molecular genetics of ketohexokinase | paediatric genetics | *Consultant(s)* | *Towns* | Skeletal dysplasia, paediatric genetics | Paediatric genetics | *Consultant(s)* | *Towns* | Paediatric genetics, renal genetics, prenatal genetics | Paediatric genetics | *Consultant(s)* | *Towns* | Paediatric genetics, cardiac genetics, rare disease genetics | paediatric genetics | *Consultant(s)* | *Towns* | Cancer genetics, paediatric genetics, neurofibromatosis type 1 | paediatric genetics | *Consultant(s)* | *Towns* | Cancer genetics, paediatric genetics, Huntington's disease | prenatal genetics | *Consultant(s)* | *Towns* | Paediatric genetics, renal genetics, prenatal genetics | rare disease genetics | *Consultant(s)* | *Towns* | Paediatric genetics, cardiac genetics, rare disease genetics | renal genetics | *Consultant(s)* | *Towns* | Paediatric genetics, renal genetics, prenatal genetics |
