M. Ireland

发表

A de novo translocation t(3;17)(q26.3;q23.1) in a child with Cornelia de Lange syndrome.

J. Burn, I. Cross, M. Ireland, 1991, Journal of medical genetics.

Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.

D. Schlessinger, J. Clayton-Smith, J. Hurst, 1997, Journal of Medical Genetics.

Genomic organisation of the human chordin gene and mutation screening of candidate Cornelia de Lange syndrome genes

T. Strachan, R. Skoda, A. Wiestner, 1999, Human Genetics.

A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3

I. Krantz, T. Strachan, S. Lindsay, 2004, Human Genetics.

De Lange syndrome: subjective and objective comparison of the classical and mild phenotypes.

R. Hennekam, J. Allanson, M. Ireland, 1997, Journal of medical genetics.

Partial trisomy 3q and the mild Cornelia de Lange syndrome phenotype.

T. Strachan, S. Lindsay, I. Cross, 1995, Journal of medical genetics.

Glypican 3 and glypican 4 are juxtaposed in Xq26.1.

R. Mazzarella, E. Chen, S. Lindsay, 1998, Gene.

Second‐trimester pregnancy associated plasma protein‐A levels are reduced in Cornelia de Lange syndrome pregnancies

J. Burn, J. Connor, J. Crossley, 1999, Prenatal diagnosis.

Radiological features in Brachmann-de Lange syndrome.

J. Graham, J. Carey, J. Moeschler, 1993, American journal of medical genetics.

Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.

D. Schlessinger, J. Clayton-Smith, J. Hurst, 1997, Journal of medical genetics.

Cornelia de Lange syndrome: clinical features, common complications and long-term prognosis

M. Ireland, 1996 .

Behavioural phenotype of Cornelia de Lange syndrome

T. Berney, J. Burn, M. Ireland, 1999, Archives of disease in childhood.

Brachmann-de Lange syndrome. Delineation of the clinical phenotype.

J. Burn, D. Donnai, M. Ireland, 1993, American journal of medical genetics.

Mapping of Simpson-Golabi-Behmel syndrome to Xq25-q27.

A. Mackenzie, J. Xuan, M. Ireland, 1994, Human molecular genetics.