K. Leask

A molecular and clinical study of Larsen syndrome caused by mutations in FLNB

S. Robertson, T. de Ravel, H. Firth, 2006, Journal of Medical Genetics.

Inherited association of breast and colorectal cancer: limited role of CHEK2 compared with high‐penetrance genes

A. Shenton, F. Lalloo, D. Speake, 2006, Clinical genetics.

MRI and neurological findings in macrocephaly-cutis marmorata telangiectatica congenita syndrome: report of ten cases and review of the literature.

J. Clayton-Smith, J. Hurst, L. Garavelli, 2005, Genetic counseling.

Cardiomyopathy with renal anomalies in two siblings: a new recessive syndrome?

B. Kerr, E. Ladusans, K. Leask, 2007, Clinical dysmorphology.

Non‐mosaic trisomy 22: a report of 2 cases

S. Mehta, S. Sharif, Audrey Smith, 2006, Prenatal diagnosis.

The role of the courts in clinical decision making

K. Leask, 2005, Archives of Disease in Childhood.

A molecular and clinical study of Larsen syndrome caused by mutations in FLNB

S. Robertson, H. Firth, D. Rimoin, 2006, Journal of Medical Genetics.