A. Gedeon

发表

Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28.

D. Sillence, J. Mulley, L. Adès, 1993, American journal of medical genetics.

Mapping the short arm of human chromosome 16.

G. Sutherland, J. Mulley, D. Callen, 1989, Genomics.

Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation.

I. Glass, J. Mulley, J. Connor, 1996, American journal of medical genetics.

Refined genetic localization for central core disease.

F. Couch, J. Mulley, R. Gregg, 1993, American journal of human genetics.

Use of linkage data obtained in single families: prenatal diagnosis of a new X-linked mental retardation syndrome.

E. Haan, J. Mulley, S. Wilson, 1992, American journal of medical genetics.

Localisation of the gene for X-linked reticulate pigmentary disorder with systemic manifestations (PDR), previously known as X-linked cutaneous amyloidosis.

A. Donnelly, J. Mulley, M. Partington, 1994, American journal of medical genetics.

The molecular basis of X-linked spondyloepiphyseal dysplasia tarda.

J. Gécz, A. Munnich, S. Robertson, 2001, American journal of human genetics.

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

D. Sillence, J. Mulley, Meredith Wilson, 1995, Journal of medical genetics.

Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14.

G. Sutherland, J. Mulley, A. Gedeon, 1987, American journal of medical genetics.

Addition of MT, D16S10, D16S4, and D16S91 to the linkage map within 16q12.1-q22.1.

G. Sutherland, J. Mulley, G. Suthers, 1991, Genomics.

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

D. Loesch, G. Sutherland, J. Mulley, 1993, American journal of human genetics.

Regional localisation of a non-specific X-linked mental retardation gene (MRX19) to Xp22.

A. Donnelly, J. Mulley, D. Danks, 1994, American journal of medical genetics.

Characterization of new PCR based markers for mapping and diagnosis: AC dinucleotide repeat markers at the DXS237 (GMGX9) and DXS102 (cX38.1) loci.

K. Holman, J. Mulley, R. Richards, 1992, American journal of medical genetics.

FRAXE and mental retardation.

D. Loesch, S. Yu, A. Donnelly, 1995, Journal of medical genetics.

Fragile X syndrome without CCG amplification has an FMR1 deletion

A. Poustka, B. Korn, S. Yu, 1992, Nature Genetics.

Predictive diagnosis of myotonic dystrophy with flanking microsatellite markers.

E. Haan, J. Mulley, S. White, 1991, Journal of medical genetics.

Fragile-X syndrome: unique genetics of the heritable unstable element.

D. Loesch, R. Richards, S. Yu, 1992, American journal of human genetics.

Linkage studies with the gene for an X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2)

E. Haan, G. Sutherland, J. Mulley, 1988, American journal of medical genetics.

A linkage map of microsatellite markers on the human X chromosome.

R. Richards, G. Sutherland, A. Donnelly, 1994, Genomics.

Experience with direct molecular diagnosis of fragile X.

D. Loesch, R. Richards, S. Yu, 1992, Journal of medical genetics.

Direct molecular diagnosis of myotonic dystrophy

E. Haan, A. Donnelly, R. Byard, 1993, Clinical genetics.

Prenatal diagnosis of fragile X syndrome by direct detection of the unstable DNA sequence.

L. Kornman, S. Yu, G. Sutherland, 1991, The New England journal of medicine.

X‐linked lymphoproliferative disease: prenatal detection of an unaffected histocompatible male

D. Ledbetter, J. Mulley, V. Berdoukas, 1992, Clinical genetics.

XmnI, HincII and BclI RFLPs at D16S79.

M. Breuning, A. Gedeon, J. Mulley, 1989, Nucleic acids research.