Agi Gedeon
Agi Gedeon
currently @ UWA
Verified email at uwa.edu.au
Title
Cited by
Cited by
Year
A novel X-linked gene, G4. 5. is responsible for Barth syndrome
S Bione, P D'Adamo, E Maestrini, AK Gedeon, PA Bolhuis, D Toniolo
Nature genetics 12 (4), 385-389, 1996
7171996
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy
P Str°mme, ME Mangelsdorf, MA Shaw, KM Lower, SME Lewis, ...
Nature genetics 30 (4), 441-445, 2002
4462002
Mutations in GDI1 are responsible for X-linked non-specific mental retardation (vol 19, pg 134, 1998)
P D'Adamo, A Menegon, C Lo Nigro, M Grasso, M Gulisano, F Tamanini, ...
NATURE GENETICS 19 (3), 303-303, 1998
378*1998
Mutations in GDI1 are responsible for X-linked non-specific mental retardation
P D'Adamo, A Menegon, CL Nigro, M Grasso, M Gulisano, F Tamanini, ...
Nature genetics 19 (2), 134-139, 1998
3781998
Identification of the gene FMR2, associated with FRAXE mental retardation
J Gecz, AK Gedeon, GR Sutherland, JC Mulley
Nature genetics 13 (1), 105-108, 1996
2991996
The X-linked gene G4. 5 is responsible for different infantile dilated cardiomyopathies
P D'Adamo, L Fassone, A Gedeon, EAM Janssen, S Bione, PA Bolhuis, ...
The American Journal of Human Genetics 61 (4), 862-867, 1997
2731997
Fragile-X syndrome: unique genetics of the heritable unstable element
S Yu, J Mulley, D Loesch, G Turner, A Donnelly, A Gedeon, D Hillen, ...
American journal of human genetics 50 (5), 968, 1992
2381992
Fragile X syndrome without CCG amplification has an FMR1 deletion
AK Gedeon, E Baker, H Robinson, MW Partington, B Gross, A Manca, ...
Nature Genetics 1 (5), 341-344, 1992
2371992
Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda
┴K Gedeon, A Colley, R Jamieson, EM Thompson, J Rogers, D Sillence, ...
Nature genetics 22 (4), 400-404, 1999
2181999
Mutations in PHF6 are associated with B÷rjeson–Forssman–Lehmann syndrome
KM Lower, G Turner, BA Kerr, KD Mathews, MA Shaw, ┴K Gedeon, ...
Nature genetics 32 (4), 661-665, 2002
1822002
Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 gene
MR Davis, E Haan, H Jungbluth, C Sewry, K North, F Muntoni, T Kuntzer, ...
Neuromuscular Disorders 13 (2), 151-157, 2003
1222003
Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28
LC Ades, AK Gedeon, MJ Wilson, M Latham, MW Partington, JC Mulley, ...
American Journal of Medical Genetics Part A 45 (3), 327-334, 1993
1201993
Prenatal diagnosis of fragile X syndrome by direct detection of the unstable DNA sequence
GR Sutherland, A Gedeon, L Kornman, A Donnelly, RW Byard, JC Mulley, ...
New England Journal of Medicine 325 (24), 1720-1722, 1991
1181991
The molecular basis of X-linked spondyloepiphyseal dysplasia tarda
AK Gedeon, GE Tiller, M Le Merrer, S Heuertz, L Tranebjaerg, D Chitayat, ...
The American Journal of Human Genetics 68 (6), 1386-1397, 2001
1132001
FRAXE and mental retardation.
JC Mulley, S Yu, DZ Loesch, DA Hay, A Donnelly, AK Gedeon, ...
Journal of medical genetics 32 (3), 162-169, 1995
971995
Genotype-phenotype relationships in fragile X syndrome: a family study.
DZ Loesch, R Huggins, DA Hay, AK Gedeon, JC Mulley, GR Sutherland
American journal of human genetics 53 (5), 1064, 1993
881993
Letter to the editor: How many X‐linked genes for non‐specific mental retardation (MRX) are there?
AK Gedeon, AJ Donnelly, JC Mulley, B Kerr, G Turner
American Journal of Medical Genetics Part A 64 (1), 158-162, 1996
791996
Erratum: Letter to the Editor: How Many X-Linked Genes for Non-Specific Mental Retardation (MRX) Are There?
AK Gedeon, AJ Donnelly, JC Mulley, B Kerr, G Turner
American Journal of Medical Genetics 66 (1), 118, 1996
79*1996
X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome.
AK Gedeon, MJ Wilson, AC Colley, DO Sillence, JC Mulley
Journal of medical genetics 32 (5), 383-388, 1995
741995
X chromosome inactivation in carriers of Barth syndrome
KH ěrstavik, RE ěrstavik, AK Naumova, P D'Adamo, A Gedeon, ...
The American Journal of Human Genetics 63 (5), 1457-1463, 1998
731998
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Articles 1–20