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Results 1-10 of 17 (Search time: 0.005 seconds).
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PreviewIssue DateTitleAuthor(s)
1997Assignment of the Human CC Chemokine Gene TARC (SCYA17) to chromosome 16q13Nomiyama, H.; Imai, T.; Kusuda, J.; Miura, R.; Callen, D.; Yoshie, O.
1999Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3Cleton-Jansen, A.; Moerland, E.; Pronk, J.; Van Berkel, C.; Apostolou, S.; Crawford, J.; Savoia, A.; Auerbach, A.; Callen, D.; Cornelisse, C.
1997Rapid detection of euchromatin by Alu-PRINS: use in clinical cytogeneticsCallen, D.; Yip, M.; Eyre, H.
1999The PISSLRE Gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancerCrawford, J.; Ianzano, L.; Savino, M.; Whitmore, S.; Cleton-Jansen, A.; Settasatian, C.; d'Apolito, M.; Seshadri, R.; Pronk, J.; Auerbach, A.; Verlander, P.; Mathew, C.; Tipping, A.; Doggett, N.; Zelante, L.; Callen, D.; Savoia, A.
1998Localisation of the human NMDAR2D receptor subunit gene (GRIN2D) to 19q13.1-qter, the NMDAR2A subunit gene to 16p13.2 (GRIN2A), and the NMDAR2C subunit gene (GRIN2C) to 17q24-q25 using somatic cell hybrid and radiation hybrid mapping panels.Kalsi, G.; Whiting, P.; Bourdelles, B.; Callen, D.; Barnard, E.; Gurling, H.
1998Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16Cavanaugh, J.; Callen, D.; Wilson, S.; Stanford, P.; Sraml, M.; Gorska, M.; Crawford, J.; Whitmore, S.; Shlegel, C.; Foote, S.; Kohonen-Corish, M.; Pavli, P.
1998A 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.
1998Comparative 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.; Doggett, N.; Callen, D.; Cassiman, J.; Matthijs, G.
1997The genome organisation of the Fanconi Anemia Group A (FAA) GeneIanzano, L.; d'Apolito, M.; Centra, M.; Savino, M.; Levran, O.; Auerbach, A.; Cleton-Jansen, A.; Doggett, N.; Pronk, J.; Tipping, A.; Gibson, R.; Mathew, C.; Whitmore, S.; Apostolou, S.; Callen, D.; Zelante, L.; Savoia, A.
1997Genomic structure and complete nucleotide sequence of the Batten Disease Gene, CLN3Mitchison, 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.