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Issue Date
Title
Author(s)
1998
Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24
Phillips, H.
;
Scheffer, I.
;
Crossland, K.
;
Bhatia, K.
;
Fish, D.
;
Marsden, C.
;
Howell, S.
;
Stephenson, J.
;
Tolmie, J.
;
Plazzi, G.
;
Eeg-Olofsson, O.
;
Singh, R.
;
Lopes-Cendes, I.
;
Andermann, E.
;
Berkovic, S.
;
Mulley, J.
1998
Construction of an ~700-kb transcript map around the Familial Mediterranean Fever locus on human chromosome 16p13.3
Centola, M.
;
Chen, X.
;
Sood, R.
;
Deng, Z.
;
Aksentijevich, I.
;
Blake, T.
;
Ricke, D.
;
Chen, X.
;
Wood, G.
;
Zaks, N.
;
Richards, N.
;
Krizman, D.
;
Mansfield, E.
;
Apostolou, S.
;
Liu, J.
;
Shafran, N.
;
Vedula, A.
;
Hamon, M.
;
Cercek, A.
;
Kahan, T.
;
et al.
1998
Febrile seizures and generalised epilepsy associated with a mutation in the Na+-channel b1 subunit gene SCN1B
Wallace, R.
;
Wang, D.
;
Singh, R.
;
Scheffer, I.
;
George Jnr., A.
;
Phillips, H.
;
Saar, K.
;
Reis, A.
;
Johnson, E.
;
Sutherland, G.
;
Berkovic, S.
;
Mulley, J.
1998
Comparative analysis of the phosphomannomutase genes PMM1, PMM2 and PMM2y: the sequence variation in the processed pseudogene is a reflection of the mutations found in the functional gene.
Schollen, E.
;
Pardon, E.
;
Heykants, L.
;
Renard, J.P.
;
Doggett, N.
;
Callen, D.
;
Cassiman, J.J.
;
Matthijs, G.
1998
Specific expression of an expansin gene during elongation of cotton fibres.
Orford, S.
;
Timmis, J.
1998
A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis.
Town, M.
;
Jean, G.
;
Cherqui, S.
;
Attard, M.
;
Forestier, L.
;
Whitmore, S.
;
Callen, D.
;
Gribouval, O.
;
Broyer, M.
;
Bates, G.
;
van't Hoff, W.
;
Antignac, C.
1998
PAK3 mutation in nonsyndromic X-linked mental retardation
Allen, K.
;
Gleeson, J.
;
Bagrodia, S.
;
Partington, M.
;
MacMillan, J.
;
Cerione, R.
;
Mulley, J.
;
Walsh, C.
1998
The identification and localisation of a human gene with sequence similarity to Polycomblike of Drosophila melanogaster
Coulson, M.
;
Robert, S.
;
Eyre, H.
;
Saint, R.
1998
Characterisation and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer
Whitmore, S.
;
Settasatian, C.
;
Crawford, J.
;
Lower, K.
;
McCallum, B.
;
Seshadri, R.
;
Cornelisse, C.
;
Moerland, E.
;
Cleton-Jansen, A.M.
;
Tipping, A.
;
Mathew, C.
;
Savnio, M.
;
Savoia, A.
;
Verlander, P.
;
Auerbach, A.
;
Van Berkel, C.
;
Pronk, J.
;
Doggett, N.
;
Callen, D.
1998
The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.
Kortschak, R.
;
Reimann, H.
;
Zimmer, M.
;
Eyre, H.
;
Saint, R.
;
Jenne, D.
Discover
Author
3
Callen, D.
3
Mulley, J.
2
Berkovic, S.
2
Doggett, N.
2
Eyre, H.
2
Phillips, H.
2
Saint, R.
2
Scheffer, I.
2
Singh, R.
2
Whitmore, S.
.
next >
Subject
9
Humans
6
Amino Acid Sequence
5
Cloning, Molecular
5
Female
5
Male
5
Sequence Homology, Amino Acid
4
Animals
4
Base Sequence
4
Pedigree
4
Sequence Analysis, DNA
.
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