Use of the PDQ system in a clinical setting.

Por Angier, J J, Beck, S L, Eyre, H J
Publicado em 1990

A rare heteromorphism of chromosome 20 and reproductive loss.

Por Romain, D R, Whyte, S, Callen, D F, Eyre, H J
Publicado em 1991

Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics.

Por Callen, D F, Eyre, H J, Ringenbergs, M L, Freemantle, C J, Woodroffe, P, Haan, E A
Publicado em 1991

The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization.

Por Callen, D F, Freemantle, C J, Ringenbergs, M L, Baker, E, Eyre, H J, Romain, D, Haan, E A
Publicado em 1990

Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4.

Por Fang, Y Y, Eyre, H J, Bohlander, S K, Estop, A, McPherson, E, Träger, T, Riess, O, Callen, D F
Publicado em 1995

Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivation.

Por Callen, D F, Eyre, H J, Dolman, G, Garry-Battersby, M B, McCreanor, J R, Valeba, A, McGill, J J
Publicado em 1995

Chromosomal localization of the human alpha-L-iduronidase gene (IDUA) to 4p16.3.

Por Scott, H S, Ashton, L J, Eyre, H J, Baker, E, Brooks, D A, Callen, D F, Sutherland, G R, Morris, C P, Hopwood, J J
Publicado em 1990