The genetic basis for periodic fever.

Por Mulley, J C
Publicado em 1999

Genetic Adaptation to Captivity and Inbreeding Depression in Small Laboratory Populations of Drosophila Melanogaster

Por Latter, BDH., Mulley, J. C.
Publicado em 1995

A BamHI RFLP at MT2A on human chromosome 16.

Por Bates, L J, Mulley, J C
Publicado em 1988

A BclI RFLP for DXS296 (VK21) near the fragile X

Por Yu, S., Suthers, G.K., Mulley, J.C.
Publicado em 1990

An MspI RFLP at D16S10.

Por Gedeon, A K, Mulley, J C, Fratini, A
Publicado em 1989

XmnI, HincII and BclI RFLPs at D16S79.

Por Gedeon, A K, Mulley, J C, Breuning, M H
Publicado em 1989

Dinucleotide repeat polymorphisms at the DXS294 and DXS300 loci in Xq26.

Por Gedeon, A K, Richards, R I, Mulley, J C
Publicado em 1991

Reduced Genetic Load Revealed by Slow Inbreeding in Drosophila Melanogaster

Por Latter, BDH., Mulley, J. C., Reid, D., Pascoe, L.
Publicado em 1995

Regional localization for HLA by recombination with a fragile site at 6p23.

Por Mulley, J C, Hay, J, Sheffield, L J, Sutherland, G R
Publicado em 1983

An Xmnl RFLP for CYP2A on chromosome 19

Por McCure, J.A., Phillips, I.R., Shephard, E.A., Mulley, J.C.
Publicado em 1991

Dinucleotide repeat polymorphisms at the D16S164, D16S168 and D16S186 loci at 16q21-q22.1.

Por Phillips, H A, Harris, P, Richards, R I, Sutherland, G R, Mulley, J C
Publicado em 1991

Predictive diagnosis of myotonic dystrophy with flanking microsatellite markers.

Por Mulley, J C, Gedeon, A K, White, S J, Haan, E A, Richards, R I
Publicado em 1991

Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21.

Por Wallace, R H, Berkovic, S F, Howell, R A, Sutherland, G R, Mulley, J C
Publicado em 1996

Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigree.

Por Suthers, G K, Manson, J I, Stern, L M, Haan, E A, Mulley, J C
Publicado em 1989

Molecular genetics of human chromosome 16.

Por Sutherland, G R, Reeders, S, Hyland, V J, Callen, D F, Fratini, A, Mulley, J C
Publicado em 1987

X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome.

Por Gedeon, A K, Wilson, M J, Colley, A C, Sillence, D O, Mulley, J C
Publicado em 1995

Mapping the human alpha globin gene complex to 16p13.2----pter.

Por Simmers, R N, Mulley, J C, Hyland, V J, Callen, D F, Sutherland, G R
Publicado em 1987

Dinucleotide repeat polymorphism at D16S287

Por Phillips, H.A., Hyland, V.J., Holman, K., Callen, D.F., Richards, R.I., Mulley, J.C.
Publicado em 1991

Genotype-phenotype relationships in fragile X syndrome: a family study.

Por Loesch, D Z, Huggins, R, Hay, D A, Gedeon, A K, Mulley, J C, Sutherland, G R
Publicado em 1993

Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers.

Por Richards, R I, Shen, Y, Holman, K, Kozman, H, Hyland, V J, Mulley, J C, Sutherland, G R
Publicado em 1991