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PreviewIssue DateTitleAuthor(s)
1998Human chemokines fractalkine (SCYD1), MDC (SCYA22) and TARC (SCYA17) are clustered on chromosome 16q13.Nomiyama, H.; Imai, T.; Kusuda, J.; Miura, R.; Callen, D.; Yoshie, O.
1997Ancient missense mutations in a new member of the RoRet gene family are likely to cause Familial Mediterranean FeverAksentijevich, I.; Centola, M.; Deng, Z.; Sood, R.; Balow, J.; Wood, G.; Zaks, N.; Mansfield, E.; Chen, X.; Eisenberg, S.; Vedula, A.; Shafran, N.; Raben, N.; Pras, E.; Pras, M.; Kastner, D.; Blake, T.; Baxevanis, A.; Robbins, C.; Krizman, D.; et al.
1997Genetics heterogeneity in familial acute myelogenous leukemia: Evidence for a second locus at chromosome 16q21-23.2Horwitz, M.; Benson, K.; Li, F.Q.; Wolff, J.; Leppert, M.; Hobson, L.; Mangelsdorf, M.; Yu, S.; Hewett, D.; Richards, R.; Raskind, W.
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.
1997Assignment of the Human CC Chemokine Gene TARC (SCYA17) to chromosome 16q13Nomiyama, H.; Imai, T.; Kusuda, J.; Miura, R.; Callen, D.; Yoshie, O.
1998Localisation of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity.Kremmidiotis, G.; Baker, E.; Crawford, J.; Eyre, H.; Nahmias, J.; Callen, D.
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.
1998ARA, a novel ABC transporter, is located at 16p13.1, is deleted in inv(16) leukemias, & is shown to be expressed in primitive hematopoietic precursors.Kuss, B.; O'Neill, G.; Eyre, H.; Doggett, N.; Callen, D.; Davey, R.
1997A high-resolution genetic map of the familial Mediterranean fever candidate region allows identification of haplotype-sharing among ethnic groupsBalow Jnr., J.; Shelton, D.; Orsborn, A.; Mangelsdorf, M.; Aksentijevich, I.; Blake, T.; Sood, R.; Gardner, D.; Liu, R.; Pras, E.; Levy, E.; Centola, M.; Deng, Z.; Zaks, N.; Wood, G.; Chen, X.; Richards, N.; Shohat, M.; Livneh, A.; Pras, M.; et al.