H. Middleton‐Price

发表

Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease

Dirk Roos, Anthony W. Segal, H Middleton-Price, 1996 .

Female twin with Hunter disease due to nonrandom inactivation of the X-chromosome: a consequence of twinning.

J. Hurst, S. Malcolm, E. Young, 1992, American journal of medical genetics.

A multipedigree linkage study of X-linked deafness: linkage to Xq13-q21 and evidence for genetic heterogeneity.

W. Reardon, L. Sandkuijl, S. Malcolm, 1991, Genomics.

Meiotic drive at the myotonic dystrophy locus?

L. Peltonen, S. Malcolm, M. Anvret, 1994, Nature Genetics.

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation

K. Davies, S. Knight, B. Oostra, 1993, Cell.

Clinical and genetic heterogeneity in X-linked deafness.

W. Reardon, S. Malcolm, L. Luxon, 1992, British journal of audiology.

Confirmation of linkage of Sjögren-Larsson syndrome to chromosome 17 in families of different ethnic origins.

H. Middleton-Price, J. Harper, M. Lacour, 1996, Journal of medical genetics.

The use of a highly informative CA repeat polymorphism within the abetalipoproteinaemia locus (4q22–24)

P. Talmud, J. Scott, C. Shoulders, 1997, Prenatal diagnosis.

Mutational analysis in UK patients with a clinical diagnosis of familial hypercholesterolaemia: relationship with plasma lipid traits, heart disease risk and utility in relative tracing

S. Humphries, E. Hawe, A. Wierzbicki, 2006, Journal of Molecular Medicine.

A molecular genetic service for diagnosing individuals with familial hypercholesterolaemia (FH) in the United Kingdom

S. Humphries, H. Middleton-Price, M. Boxer, 2001, European Journal of Human Genetics.