Currnet Protocols in Human Genetics

Por Kearney, L, Walley, A, Ward, C, Harris, A
Publicado em 1995

“More than skin deep”: Recurrent primary hand abscesses in a warehouse operative

Por Kearney, L., O’Connor, C., Fitzpatrick, F., O’Sullivan, J. B.
Publicado no Case Reports Plast Surg Hand Surg (2015)

Fragile X syndrome.

Por McKinley, M J, Nicolaides, K H, Kearney, L U, Heron, O
Publicado em 1987

Molecular-cytogenetic detection of a deletion of 1p36.3.

Por Giraudeau, F, Aubert, D, Young, I, Horsley, S, Knight, S, Kearney, L, Vergnaud, G, Flint, J
Publicado em 1997

Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements.

Por Horsley, S W, Knight, S J, Nixon, J, Huson, S, Fitchett, M, Boone, R A, Hilton-Jones, D, Flint, J, Kearney, L
Publicado em 1998

OP14 GENETIC AND FUNCTIONAL DIVERSITY OF PROPAGATING CELLS IN GLIOBLASTOMA

Por Piccirillo, S.G.M., Colman, S., Potter, N., van Delft, F., Lillis, S., Carnicer, M., Kearney, L., Watts, C., Greaves, M.
Publicado no Neuro Oncol (2015)

A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1.

Por Johnson, D, Horsley, S W, Moloney, D M, Oldridge, M, Twigg, S R, Walsh, S, Barrow, M, Njølstad, P R, Kunz, J, Ashworth, G J, Wall, S A, Kearney, L, Wilkie, A O
Publicado em 1998

Prospective development and validation of a model to predict heart failure hospitalisation

Por Cubbon, R M, Woolston, A, Adams, B, Gale, C P, Gilthorpe, M S, Baxter, P D, Kearney, L C, Mercer, B, Rajwani, A, Batin, P D, Kahn, M, Sapsford, R J, Witte, K K, Kearney, M T
Publicado em 2014