M. Dillon

DELETION ON THE X CHROMOSOME DETECTED BY DIRECT DNA ANALYSIS IN ONE OF TWO UNRELATED BOYS WITH GLYCEROL KINASE DEFICIENCY, ADRENAL HYPOPLASIA, AND DUCHENNE MUSCULAR DYSTROPHY

M. Pembrey, D. Dunger, K. Davies, 1986, The Lancet.

Ellis-van creveld syndrome, Jeune syndrome, and renal-hepatic-pancreatic dysplasia: separate entities or disease spectrum?

R. Winter, L. Brueton, M. Dillon, 1990, Journal of medical genetics.

Further case of Rubinstein–Taybi syndrome due to a deletion in EP300

S. Lynch, P. Foley, D. Bunyan, 2009, American journal of medical genetics. Part A.

Sibs with mental retardation, supraorbital sclerosis, and metaphyseal dysplasia: frontometaphyseal dysplasia, craniometaphyseal dysplasia, or a new syndrome?

W. Reardon, C. Hall, M. Baraitser, 1991, Journal of medical genetics.

Autosomal recessive hypoparathyroidism with renal insufficiency and developmental delay.

G. Karbani, N. Shaw, M. Dillon, 1991, Archives of disease in childhood.