D. Lahey

Genetic Diagnostic Testing for Inherited Cardiomyopathies: Considerations for Offering Multi-Gene Tests in a Health Care Setting.

M. Ghani, J. McGowan-Jordan, R. Roberts, 2019, The Journal of molecular diagnostics : JMD.

Two females with mutations in USP9X highlight the variable expressivity of the intellectual disability syndrome.

L. Gallagher, K. Boycott, G. Baynam, 2017, European journal of medical genetics.

Watson syndrome: is it a subtype of type 1 neurofibromatosis?

J. Allanson, P. Harper, M. Upadhyaya, 1991, Journal of medical genetics.

A comparison of the caffeine halothane muscle contracture test with the molecular genetic diagnosis of malignant hyperthermia.

R. Korneluk, D. Maclennan, R. Worton, 1991, Anesthesiology.

A711 A COMPARISON OP THE CAFFEINE HALOTHANE CONTRACTURE TEST WITH MOLECULAR GENETICS DIAGNOSIS OF MALIGNANT HYPERTHERMIA (MH)

R. Korneluk, D. Maclennan, R. Worton, 1990 .

Watson syndrome: is it a subtype of type 1 neurofibromatosis?

J. Allanson, P. Harper, M. Upadhyaya, 1991, Journal of medical genetics.