R. Mueller

发表

Andersen–Tawil syndrome

F. Lehmann-Horn, M. G. Hanna, P. F. Chinnery, 2005, Neurology.

Assessment of the genetic causes of recessive childhood non‐syndromic deafness in the UK – implications for genetic testing

M. Bitner-Glindzicz, G. Taylor, E. Telford, 2005, Clinical genetics.

Familial Down syndrome: evidence supporting cytoplasmic inheritance

H. Cuckle, S. Arbuzova, R. Mueller, 2001, Clinical genetics.

Genetic Counseling: Consanguinity

R. Mueller, 2006 .

The prevalence of Fragile‐X syndrome in an institution for people with learning disability

R. Mueller, J. O'Dwyer, J. Holmes, 1997, Psychiatric genetics.

Hereditary metabolic myopathy with paroxysmal myoglobinuria due to abnormal glycolysis1

L. Larsson, H. Linderholm, R. Mueller, 1964, Journal of neurology, neurosurgery, and psychiatry.

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

K. Elbedour, R. Carmi, C. Srisailapathy, 1998, Human mutation.

The contribution of USH1C mutations to syndromic and non‐syndromic deafness in the UK

M. Bitner-Glindzicz, S. Malcolm, S. Bhattacharya, 2003, Clinical genetics.

Genetic linkage analysis of chromosome 19 markers in malignant hyperthermia.

A. Stewart, P. Hopkins, H. Dorkins, 1993, British journal of anaesthesia.

A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23–q31

L. Al-Gazali, N. Lench, N. Lench, 2000, European Journal of Human Genetics.

Periodic paralysis, malignant ventricular arrhythmia and dysmorphism (Andersen's syndrome): A skeletal muscle potassium channel disorder

P. Chinnery, M. Hanna, D. Hilton‐Jones, 2002 .