Nigel Smith

17q12 microdeletion syndrome: Three patients illustrating the phenotypic spectrum

R. Harrison, S. Hulton, K. Yates, 2012, American Journal of Medical Genetics. Part A.

A magnetic colloid system for isolation of rare cells from blood for FISH analysis

L. Durrant, Nigel Smith, B. Martin, 1997, Prenatal diagnosis.

Mild phenotype in a patient with a de-novo 2.9-Mb interstitial deletion at 13q12.11

A. Dixit, K. Martin, M. Suri, 2011, Clinical dysmorphology.

17q12 microdeletion syndrome: Three patients illustrating the phenotypic spectrum

R. Harrison, S. Hulton, A. Dixit, 2012, American journal of medical genetics. Part A.