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Results 1-10 of 15 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
1997
Genomic structure and complete nucleotide sequence of the Batten Disease Gene, CLN3
Mitchison, H.
;
Munroe, P.
;
O'Rawe, A.
;
Taschner, P.
;
De Vos, N.
;
Kremmidiotis, G.
;
Lensink, I.
;
Munk, A.
;
D'Arigo, K.
;
Anderson, J.
;
Lerner, T.
;
Moyzis, R.
;
Callen, D.
;
Breuning, M.
;
Doggett, N.
;
Gardiner, R.
;
Mole, S.
1995
Mechanisms of small ring formation suggested by the molecular characterization of 2 small accessory ring chromosomes derived from chromosome 4
Fang, Y.
;
Eyre, H.
;
Bohlander, S.
;
Estop, A.
;
McPherson, E.
;
Trager, T.
;
Riess, O.
;
Callen, D.
1995
Assignment of the human skeletal muscle a-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridization
Eyre, H.
;
Akkari, P.
;
Wilton, S.
;
Callen, D.
;
Baker, E.
;
Laing, N.
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.
1995
Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation
Hunt, C.
;
Eyre, H.
;
Akkari, P.
;
Meredith, C.
;
Dorosz, S.
;
Wilton, S.
;
Callen, D.
;
Laing, N.
;
Baker, E.
1996
Molecular cloning of the cDNA and chromosome localization of the gene for human ubiquitin-conjugating enzyme 9
Wang, Z.
;
Qiu, Q.
;
Seufert, W.
;
Taguchi, T.
;
Testa, J.
;
Whitmore, S.
;
Callen, D.
;
Welsh, D.
;
Shenk, T.
;
Deuel, T.
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.
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.
1999
Genomic structure and expression analysis of the spastic paraplegia gene, SPG7
Settasatian, C.
;
Whitmore, S.
;
Crawford, J.
;
Bilton, R.
;
Cleton-Jansen, A.M.
;
Sutherland, G.
;
Callen, D.
1995
Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: demonstration of a 'hot-spot' for recombination at 16p12
Callen, D.
;
Lane, S.
;
Kozman, H.
;
Kremmidiotis, G.
;
Whitmore, S.
;
Lowenstein, M.
;
Doggett, N.
;
Kenmochi, N.
;
Page, D.
;
Maglott, D.
;
Nierman, W.
;
Murakawa, K.
;
Sikela, J.
;
Houlgatte, R.
;
Auffray, C.
;
Sutherland, G.
Discover
Author
10
Whitmore, S.
7
Doggett, N.
6
Cleton-Jansen, A.M.
6
Crawford, J.
6
Savoia, A.
4
Auerbach, A.
4
d'Apolito, M.
4
Eyre, H.
4
Mathew, C.
4
Pronk, J.
.
next >
Subject
15
Humans
11
Base Sequence
8
Chromosomes, Human, Pair 16
6
Chromosome Mapping
6
Cloning, Molecular
6
Exons
5
Amino Acid Sequence
4
Animals
4
Breast Neoplasms
4
Cosmids
.
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Date issued
3
1999
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1998
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1997
2
1996
4
1995