Caroline Law

Delineation of two distinct 6p deletion syndromes

Angela Davies, Ghazala Mirza, Gurbax S. Sekhon et al. · Human Genetics · 1999 · 113 citations

Down Syndrome, Mendelian Disorder, Genetic Disorder +5

BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects

Emma Hilton, Jennifer J. Johnston, Sandra Whalen et al. · European Journal of Human Genetics · 2009 · 108 citations · Full text

Bcor Analysis, Clinical Disorders, Ophthalmology +5

Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation

David A. Koolen, William Reardon, Elisabeth Rosser et al. · European Journal of Human Genetics · 2005 · 47 citations · Full text

Molecular Characterisation, Genetic Disorder, Medicine +11

Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11

Kamini Kalidas, Adam Shaw, Andrew H. Crosby et al. · Journal of Human Genetics · 2004 · 29 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +7

Axenfeld anomaly and retinal changes in Ramon syndrome: Follow-up of two sibs

Ben Parkin, Caroline Law · American Journal of Medical Genetics · 2001 · 14 citations