Mark Ireland

Behavioural phenotype of Cornelia de Lange syndrome

T. P. Berney, Mark Ireland, John Burn · Archives of Disease in Childhood · 1999 · 145 citations · Full text

Postal Questionnaire, Pathology, Social Sciences +17

Brachmann‐de Lange syndrome. Delineation of the clinical phenotype

Mark Ireland, Dian Donnai, John Burn · American Journal of Medical Genetics · 1993 · 112 citations

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

Judith Allanson, Raoul C. M. Hennekam, Mark Ireland · Journal of Medical Genetics · 1997 · 89 citations · Full text

Corticobasal Degeneration, Immunodeficiencies, Immunology +23

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

Mark Ireland, Carol English, I Cross et al. · Journal of Medical Genetics · 1991 · 80 citations · Full text

Developmental Anomaly, Developmental Biology, Genetic Disorder +12

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

Susan Lindsay, Mark Ireland, Ottie O’Brien et al. · Journal of Medical Genetics · 1997 · 66 citations · Full text