Defects and their structure in nonmetallic solids /

Por Henderson, B., Hughes, A. E.
Publicado em c197

Segregation distortion in myotonic dystrophy.

Por Magee, A C, Hughes, A E
Publicado em 1998

Fine localisation of the gene for central areolar choroidal dystrophy on chromosome 17p.

Por Hughes, A E, Lotery, A J, Silvestri, G
Publicado em 1998

Complement in age-related macular degeneration: a focus on function

Por Bradley, D T, Zipfel, P F, Hughes, A E
Publicado em 2011

Association of two loci on chromosome 2q with nodal osteoarthritis.

Por Wright, G D, Hughes, A E, Regan, M, Doherty, M
Publicado em 1996

Duchenne muscular dystrophy in a female with a translocation involving Xp21.

Por Nevin, N C, Hughes, A E, Calwell, M, Lim, J H
Publicado em 1986

Association study of detoxification genes in age related macular degeneration

Por Esfandiary, H, Chakravarthy, U, Patterson, C, Young, I, Hughes, A E
Publicado em 2005

Linkage of epidermolysis bullosa simplex to keratin gene loci.

Por McKenna, K E, Hughes, A E, Bingham, E A, Nevin, N C
Publicado em 1992

Quantifying ultra-rare pre-leukemic clones via targeted error-corrected sequencing

Por Young, A L, Wong, T N, Hughes, A E O, Heath, S E, Ley, T J, Link, D C, Druley, T E
Publicado no Leukemia (2015)

Excess congenital non-synonymous variation in leukemia-associated genes in MLL− infant leukemia: a Children's Oncology Group report

Por Valentine, M C, Linabery, A M, Chasnoff, S, Hughes, A E O, Mallaney, C, Sanchez, N, Giacalone, J, Heerema, N A, Hilden, J M, Spector, L G, Ross, J A, Druley, T E
Publicado em 2014