Addressing key issues in the consanguinity-related risk of autosomal recessive disorders in consanguineous communities: lessons from a qualitative study of British Pakistanis

Por Darr, A., Small, N., Ahmad, W. I. U., Atkin, K., Corry, P., Modell, B.
Publicado no J Community Genet (2015)

High-frequency dielectric spectroscopy of concentrated membrane suspensions.

Por Kirkpatrick, D S, McGinness, J E, Moorhead, W D, Corry, P M, Proctor, P H
Publicado em 1978

Examining the family-centred approach to genetic testing and counselling among UK Pakistanis: a community perspective

Por Darr, A., Small, N., Ahmad, W. I. U., Atkin, K., Corry, P., Benson, J., Morton, R., Modell, B.
Publicado em 2012

Radiobiological impact of dose calculation algorithms on biologically optimized IMRT lung stereotactic body radiation therapy plans

Por Liang, X., Penagaricano, J., Zheng, D., Morrill, S., Zhang, X., Corry, P., Griffin, R. J., Han, E. Y., Hardee, M., Ratanatharathom, V.
Publicado no Radiat Oncol (2016)

Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variation

Por Roberts, E, Hampshire, D, Pattison, L, Springell, K, Jafri, H, Corry, P, Mannon, J, Rashid, Y, Crow, Y, Bond, J, Woods, C
Publicado em 2002

Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter.

Por Jackson, A P, McHale, D P, Campbell, D A, Jafri, H, Rashid, Y, Mannan, J, Karbani, G, Corry, P, Levene, M I, Mueller, R F, Markham, A F, Lench, N J, Woods, C G
Publicado em 1998

Aicardi-Goutières Syndrome Displays Genetic Heterogeneity with One Locus (AGS1) on Chromosome 3p21

Por Crow, Y. J., Jackson, A. P., Roberts, E., van Beusekom, E., Barth, P., Corry, P., Ferrie, C. D., Hamel, B. C. J., Jayatunga, R., Karbani, G., Kálmánchey, R., Kelemen, A., King, M., Kumar, R., Livingstone, J., Massey, R., McWilliam, R., Meager, A., Rittey, C., Stephenson, J. B. P., Tolmie, J. L., Verrips, A., Voit, T., van Bokhoven, H., Brunner, H. G., Woods, C. G.
Publicado em 2000