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Results 21-30 of 45 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
1997
FMR2 expression in families with FRAXE mental retardation
Gecz, J.
;
Oostra, B.
;
Hockey, A.
;
Carbonell, P.
;
Turner, G.
;
Haan, E.
;
Sutherland, G.
;
Mulley, J.
1995
Molecular basis of p(CCG)n repeat instability at the FRA16A fragile site locus
Nancarrow, J.
;
Holman, K.
;
Hori, T.
;
Denton, M.
;
Sutherland, G.
;
Richards, R.
1995
Molecular dissection of a contiguous gene syndrome: Localization of the genes involved in the Langer-Giedion syndrome
Ludecke, H.J.
;
Wagner, M.
;
Nardmann, J.
;
La Pillo, B.
;
Parrish, J.
;
Willems, P.
;
Sutherland, G.
1997
AMP-activated protein kinase isoenzyme family: subunit structure and chromosomal location
Stapleton, D.
;
Woollatt, E.
;
Mitchelhill, K.
;
Nicholl, J.
;
Fernandez, C.
;
Michell, B.
;
Witters, L.
;
Power, D.
;
Sutherland, G.
;
Kemp, B.
1997
Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat
Yu, S.
;
Mangelsdorf, M.
;
Hewett, D.
;
Hobson, L.
;
Baker, E.
;
Eyre, H.
;
Lapsys, N.
;
Le Paslier, D.
;
Doggett, N.
;
Sutherland, G.
;
Richards, R.
1996
Positional cloning of the Fanconi anaemia group A gene
Apostolou, S.
;
Whitmore, S.
;
Crawford, J.
;
Lennon, G.
;
Sutherland, G.
;
Callen, D.
;
Ianzano, L.
;
Savino, M.
;
d'Apolito, M.
;
Notarangelo, A.
;
Memeo, E.
;
Piemontese, M.
;
Zelante, L.
;
Savoia, A.
;
Gibson, R.
;
Tipping, A.
;
Morgan, N.
;
Hassock, S.
;
Jansen, S.
;
de Ravel, T.
;
et al.
1995
Cloning of the sulphamidase gene and identification of mutations in Sanfilippo A syndrome
Scott, H.
;
Blanch, L.
;
Guo, X.H.
;
Freeman, C.
;
Orsborn, A.
;
Baker, E.
;
Sutherland, G.
;
Morris, C.
;
Hopwood, J.
1998
FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis
Hewett, D.
;
Handt, O.
;
Hobson, L.
;
Mangelsdorf, M.
;
Eyre, H.
;
Baker, E.
;
Sutherland, G.
;
Schuffenhauer, S.
;
Mao, J.I.
;
Richards, R.
1995
Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2
Jones, C.
;
Penny, L.
;
Mattina, T.
;
Yu, S.
;
Baker, E.
;
Voullaire, L.
;
Langdon, W.
;
Sutherland, G.
;
Richards, R.
;
Tunnacliffe, A.
1995
A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
Steinlein, O.
;
Mulley, J.
;
Propping, P.
;
Wallace, R.
;
Phillips, H.
;
Sutherland, G.
;
Scheffer, I.
;
Berkovic, S.
Discover
Author
16
Baker, E.
11
Eyre, H.
8
Nicholl, J.
7
Woollatt, E.
4
Crawford, J.
4
Lanier, L.
4
Phillips, J.
4
Richards, R.
3
Callen, D.
3
Doggett, N.
.
next >
Subject
44
Humans
35
Base Sequence
30
Chromosome Mapping
29
Amino Acid Sequence
24
Animals
23
Cloning, Molecular
19
In Situ Hybridization, Fluorescence
16
Male
14
DNA, Complementary
13
Mice
.
next >
Date issued
9
1999
6
1998
7
1997
9
1996
14
1995