Scientific Commons: Lesley Carole Ades

Preferential pre-mRNA utilisation of an upstream cryptic 5' splice site created by a single base deletion mutation in exon 37 of the FBN-1 gene (1998)

Gibson, M. A., Ellis, S. L., Ades, Lesley Carole, Haan, E., Cleary, E. G.

Preferential pre-mRNA utilisation of an upstream cryptic 5' splice site created by a single base deletion mutation in exon 37 of the FBN-1 gene (1998)

Gibson, M. A., Ellis, S. L., Ades, Lesley Carole, Haan, E., Cleary, E. G.

A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome (1997)

Muenke, M., Gripp, K. W., McDonald-McGinn, D. M., Gaudenz, K., Whitaker, L. A., Bartlett, S. P., ...

Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene (1997)

Collod-Beroud, G., Beroud, C., Ades, Lesley Carole, Black, C., Boxer, M., Brock, D. J., ...

A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome (1997)

Muenke, M., Gripp, K. W., McDonald-McGinn, D. M., Gaudenz, K., Whitaker, L. A., Bartlett, S. P., ...

Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene (1997)

Collod-Beroud, G., Beroud, C., Ades, Lesley Carole, Black, C., Boxer, M., Brock, D. J., ...

Clinicopathologic features of congenital aneurysms of the great vessels (1996)

Ades, Lesley Carole, Knight, W. B., Byard, Roger William, Bateman, J. F., Esquivel, J. A. D., Mee, R. B. B., ...

Characterisation of four novel fibrillin-1 mutations in the Marfan syndrome (1996)

Ades, Lesley Carole, Haan, E A., Colley, A F., Richards, Robert Ian

Forty-four percent of the fibrillin-1 gene (FBN1) from 19 unrelated families with Marfan syndrome was screened for putative mutations by single strand conformational polymorphism (SSCP) analysis....

Clinicopathologic features of congenital aneurysms of the great vessels (1996)

Ades, Lesley Carole, Knight, W. B., Byard, R. W., Bateman, J. F., Esquivel, J. A. D., Mee, R. B. B., ...

Characterisation of four novel fibrillin-1 mutations in the Marfan syndrome (1996)

Ades, Lesley Carole, Haan, E A., Colley, A F., Richards, Robert Ian

Forty-four percent of the fibrillin-1 gene (FBN1) from 19 unrelated families with Marfan syndrome was screened for putative mutations by single strand conformational polymorphism (SSCP) analysis....

Overlapping submicroscopic deletions in Xq28 in two unrelated boys with developmental disorders: Identification of a gene near FRAXE (1995)

Gedeon, A. K., Keinanen, M., Ades, Lesley Carole, Kaariainen, H., Gecz, J., Baker, E., ...

The natural history of basilar impression in osteogenesis imperfecta. Correlation with 01 type (1995)

Sillence, D. O., Joshi, R., Ogle, R., Turner, A., Ades, Lesley Carole, Wilson, M., ...

Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndrome (1995)

Ades, Lesley Carole, Morris, L. L., Power, R. G., Wilson, M., Haan, E. A., Bateman, J. F., ...

Myocardial infarction resulting from coronary artery dissection in an adolescent with Ehlers-Danlos syndrome type IV, due to a type III collagen mutation (1995)

Ades, Lesley Carole, Waltham, R. D., Chiodo, A. A., Bateman, J. F.

A region of primer binding variation at the D6S265 locus associated with HLA-A25 and HLA-A26 antigens (1995)

Pyper, W. R., Burt, M. J., Powell, L. W., Webb, S. I., Ades, Lesley Carole, Halliday, J. W., ...

Localization of craniosynostosis Adelaide type to 4p16 (1995)

Hollway, G. E., Phillips, H. A., Ades, Lesley Carole, Haan, E. A., Muley, J. C.